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<![CDATA[Research laboratory at Duke is looking for a data technician. Part time, 20hr/week, hourly position. Job Description: Telephone surveys, data entry, meeting with adult and college smokers to complete surveys. Education: Bachelors degree Experience: Some experience in data entry preferred. Skills: Excellent telephone and interpersonal communication skills. Experience with telephone surveys and data entry preferred. Begins December 15, 2008. Must be able to work afternoons/early evenings 5 days/week. Please send CV/cover letter via email with address line "DataTech". ]]>

<![CDATA[Axiom Environmental, Inc. is looking for a motivated individual for full-time employment with benefits to assist with stream and wetland monitoring and design, jurisdictional area delineations, threatened and endangered species surveys, and technical writing. Individual will be responsible for groundwater monitoring at several wetland mitigation sites and will assist with numerous other office and field tasks that will require travel, both day and overnight trips. Knowledge of Microsoft Word and Microsoft Excel are a must; experience with ArcView, Microstation, surveying equipment, and/or groundwater monitoring devices are a plus. Experience/Education: B.A./B.S. in environmental science, natural resources, or other related field with general knowledge of flora and fauna of North Carolina, soils, wetlands, stream restoration principles, and/or groundwater hydrology very helpful.]]>

<![CDATA[Are you looking for an Executive Administrative Assistant with an excellent company? Do you have 10+ years experience supporting an CEO? If so, please apply to the job post. *Coordinate and lead CEO and other executive administrative assistants, work independently, be highly experienced in coordinating complex travel arrangements and reconciling expense reports, ability to handle detailed electronic calendar, must be able to work flexible hours, travel occasionally as needed to support executive officer and board level meetings. This is a temp-perm position after 90 days. Please attach a resume. *Flexible, multi-tasker, self-starter, professional, and able to work with many diverse personalities. *10+ years experience supporting a CEO. Pharmaceutical experience is required. *Master in Word, Excel and PowerPoint. *Excellent oral and written communication skills.]]>

<![CDATA[SWA Consulting Inc. (SWA) has an opening for a full-time Entry-Level Data Specialist position. This position is a great opportunity for a recent graduate who has earned a BS/BA and is interested in getting applied research experience. SWA encourages the use of organizational data for student research and publications. Relevant on-the-job training will be provided. Role Responsibilities: <ul> <li>Peform various duties related to data processing, including data collection, form development, sorting and disassembling questionnaires, scanning forms, cleaning data, and tracking and organizing study variables in a codebook</li> <li>Conduct basic item-level and descriptive statistics</li> </ul> Qualifications: <blockquote>Required <ul> <li>BS/BA in Psychology, Sociology, or related field</li> <li>Ability to work independently or as part of a team</li> <li>Being a self-starter and self-motivated to complete project goals</li> <li>Ability to handle multiple projects</li> <li>Attention to detail</li> <li>Enthusiasm to cross-train and develop new skill sets</li> <li>U.S. citizenship (because most of the work will be on a government contract)</li> </ul> Preferred <ul> <li>Previous work experience including statistical analysis, survey design, data collection, and report processing</li> <li>Proficiency in SPSS or other statistical programming package</li> <li>Experience with MS Office tools, including Excel, Word, PowerPoint</li> <li>Strong critical appraisal, analytical, writing, and research skills</li> <li>A familiarity with training research, criterion development, research design, testing, data collection methods, language testing or language training</li> </ul> </blockquote> Company Background: SWA is an organizational consulting and personnel research firm based in Raleigh, NC. Since 1997, SWA has been applying the principles, research, and methods of industrial/organizational (I/O) psychology to assist organizations and their employees in enhancing their performance, solving work-related problems, and addressing workplace issues. SWA consults and conducts research in areas related to (1) training and development, (2) performance measurement and management, (3) organizational effectiveness and development, (4) human resources development and management, and (5) work-related language proficiency, performance assessment, and training. One of SWA’s areas of specialization relates to the measurement of foreign or second language proficiency and the evaluation and effectiveness of foreign or second language training, training tools, and job aids in work contexts. ]]>

<![CDATA[Primary responsibilities will include: authorship of adverse event narratives, obtaining medically relevant follow up information on case reports, classification of adverse events according to US and international reporting requirements, identification and coding of adverse event terms in MedDRA, and reviewing information entered into the global database for accuracy and completeness. He/she will provide back up support to other Drug Safety Scientists and Drug Safety Coordinators in the processing of spontaneous and clinical trial adverse events. ]]>

<![CDATA[BioMedomics is a privately-held bioscience and medical device company with facilities in RTP that develops and sells advanced research and clinical reagents, assay instruments and data processing tools. The company’s commercial products and services meet the needs of a broad range of biomedical applications related to drug discovery and development, as well as clinical diagnostics. In order to meet the needs of its growth and exciting business opportunities, BioMedomics is looking for motivated full-time (or part-time) medical diagnostic product development staff with biochemistry and bioengineering background and experience. Job Description: Work with company’s other scientists and engineers, as well as outside contract company staff members to engage medical diagnostics product development. The following experiences and working background are preferred: protein based diagnostics technology development, lateral flow immunoassays, nanoparticles, surface chemistry, biodetection, and FDA regulation process related to medical diagnostic devices. In addition, works independently, requires minimal supervision. Excellent communication and organizational skills with biomedical clinical diagnostics. Need working permission in US. Contact: If you have interest for this challenging job, please send your resume information to fwang@biomedomics.com.]]>

<![CDATA[Master of Public Health in Biostatistics, Bachelor of Science in Mathematics with 3+ years of relative statistical and SAS programming experience. If you are in need of a statistical consultant, please send me an email with a brief summary of your statistical needs. Resume available upon request. Hourly rate is negotiable. ]]>

<![CDATA[-Maintains controlled documents: Standard Operating Procedures (SOPs), Work Practice Documents(WPDs) -Manages creation, revision and retirement of controlled documents – with increasing complexity and work on higher priority projects as level increases -Performs administrative tasks for the Office of Quality Assurance -Handles record retention issues -Maintains training files for all RTI-HS employees -Non-managerial -Reviews and edits controlled documents -Manages record retention process -Applies and interprets standard scientific or engineering theories, concepts and techniques. Develops solutions to problems where established theories and techniques can be identified and some precedents exist. Expected to use familiar processes to complete work assignments. Activities are checked and work is reviewed for accuracy, completeness, and soundness of technical judgment -Performs research tasks of limited technical complexity, applying standard and established theories, concepts, and techniques occasionally employing innovative approaches or analyses. Prepares reports and report chapters that demonstrate organization, clarity, and proper format. Work is performed under the supervision of project leaders or other more experienced researchers. Requirements: -Bachelor's Degree in a science-related field -At least 6 months of experience working with Controlled Documents *This is a 3 month contract position. *The candidate in this position does have the opportunity to be considered for a full time position. ]]>

<![CDATA[Want to work in an interactive, fast-paced, team environment? My client, who is developing some unique technology with pharmaceutical development applications has an immediate need for an experience software engineer (full time position): The software engineer with be working with other software developers and scientists in developing and maintaining scientific analysis/statistical tools including peak detection/analysis and visualization tools. Requirements - MS or Ph.D. degree in Biology, Chemistry, or equivalent. 5+ years of direct pharmaceutical/laboratory applications experience (important - you must have experience in working directly in providing laboratory applications support and have worked directly with other scientists in the development of software) Must have algorithm development, computer programming, and statistical programming experience (C++, C# preferred) as well as be highly proficient in Oracle PL/SQL. Must have excellent communication skills and able to take the lead on projects and work effectively with other scientists. For immediate consideration, please submit your resume in Word format. Only local RTP, NC candidates will be considered.]]>

<![CDATA[PERFECT THE PROCESS CONTRIBUTE AND COMMUNICATE SHARE KNOWLEDGE CREATE THE FUTURE SENIOR RECOVERY RESEARCH ENGINEER What kind of difference can you make in the future? At Novozymes, we use bio-innovation to solve industrial problems today and prepare industry for the demands of tomorrow. We lead the way in finding sustainable solutions for a variety of industrial processes including biofuels, brewing, detergents and much more. At Novozymes, we have a unique company culture – one of openness and passion, spark and science. We are committed to creating exciting jobs and providing development opportunities in a stimulating international working environment. This is your chance! Join us on the road to the future – creating better business, a cleaner environment and better quality of life. This position will have a focused effort on the optimization of downstream production processes to reduce the variable cost, liberate capacity and/or improve the product quality Responsibilities: • Downstream process optimization resulting in incremental or step changes • Small and large scale trials • Implementation of optimized processes in production • Existing technology optimization • Project management of optimization projects • Design of experiments, organize data, and critically analyze the results Requirements: • PhD in Chemical Engineering or Biochemical Engineering with 0+ years related experience (a MS in Chemical Engineering or Biochemical Engineering with 3+ years related experience will also be considered) • Knowledge of protein recovery, filtration equipment, and crystal dissolution • Previous project management experience preferred We are looking for a candidate who displays a hands-on approach to process optimization and troubleshooting, which is self-motivating, a team player and has strong organization and interpersonal skills. The successful candidate should have a proven track record of the ability to deliver results on time. If you would like to be considered for this exciting opportunity, go to Novozymes.com/Careers (search for positions in Franklinton, NC) to forward your resume/cover letter. Preference will be given to candidates not requiring sponsorship to work in the United States. Affirmative Action/Equal Opportunity Employer. M/F/D/V.]]>

<![CDATA[Do you enjoy teaching science to middle school students? Do you have basic computer programming skills? Do you have an interest in robotics? If so, we (non-profit) are looking for a science and computer programming oriented person to teach middle school studnets after school. This is a part-time job, but could become full time if desired.]]>

<![CDATA[Need person to review batch records and cGMP documentation. This position is for at leased 6 months with great chances of extending to 1 full year plus. (depending on need and performance). Experience preferred in QA document verification (calculations and GMP). Must be very familiar with cGMP guidelines. We value experience as well as education (one could compensate the other) Most speak, write, and communicate clearly in English. email resume in MS Word to info@biothermalllc.com with bill rate per hour]]>

<![CDATA[Optical Coherence tomography (OCT) is an exciting non-invasive, cutting edge technology that allows one to evaluate the anatomy and thickness characteristics of the retina in real-time in the living organism. It can be thought of as a form of in vivo histology. Increasingly, optical coherence tomography has been used by clinicians to help diagnose and manage a variety of ocular disorders, including macular degeneration, diabetic retinopathy, and glaucoma, the leading causes of blindness in the United States and around the world. There has been an explosion of interest by pharmaceutical companies to develop new treatments for macular degeneration, diabetic retinopathy, and other retinal diseases. These companies have extensively incorporated OCT as a key retinal imaging modality during conduct of these pharmacological trials. The OCT Reading Center at Duke was founded in 2001 to acquire and interpret OCT images from clinical study sites for sponsored clinical trials, to develop OCT imaging and interpretation protocols that serve as industry and clinical standards, and to produce high quality research data that will favorably impact patient care. We are providing an exciting full-time job opportunity to work as a technical analyst at the OCT Reading Center at Duke. The work is conducted in an interactive, attractive environment. As a technical analyst, the individual will have responsibilities that include, but are not limited to the following: • Grade OCT images according to OCT Reading Center protocols • Provide feedback to the Senior Technical Analyst, Project Manager and study sites regarding the quality of images submitted. • Help to certify study site OCT technicians. • Perform OCT technician evaluations and prepare OCT technician evaluation reports. • Help to develop and implement policies and procedures as needed. • Assist with standard operating procedure updates as needed. • Help the Senior Technical Analyst to develop and maintain electronic grading systems. • Verify and audit data entered • Perform data entry • Compare and transcribe Reader forms • Enhance and implement the OCT Reading Center at Duke Data Transmission Site (DTS), and train site technicians. • Keep abreast of new developments and techniques in the field and recommend modifications to existing systems as necessary to improve quality and efficiency; and to adapt to specific requirements for clinical and research activities. • Perform other related duties incidental to the work described herein. MINIMUM HIRING SPECIFICATIONS Work requires a Bachelor of Science (or equivalent) degree. Computer literacy is essential, although specific familiarity with OCT is not required. The individual should enjoy interacting with others, like to troubleshoot problems, and be willing to accept new challenges. Please reply to this post with your resume or CV attached. Your attachment should have your name in the file name. ]]>

<![CDATA[Landscape Information Scientist Waratah Corporation Description: Waratah Corporation is a high-technology software business specializing in statistical software products and services. The Waratah RTP office is looking for a candidate with experience in landscape sciences, spatial methods and data analysis. Candidates should have some experience and/or exposure to ArcInfo/ArcView and/or S-PLUS/R/SAS. Web programming skills e.g. HTML/XML, asp/jsp and/or project management experience are a plus. The primary responsibility of the position involves working closely with the EPA on a landscape ecology project identifying regions of vulnerability with applications to land use planning. Some tasks include project management and communication regarding use of Waratah-developed web-based software and data analysis methods for regional planning. The position includes some travel to EPA regional offices as part of collaboration between EPA research and regional offices. Candidate should have scientific training in the environmental sciences with coursework/experience in landscape ecology and/or environmental policy, and an interest in the application of landscape sciences to solve real world management problems. The candidate should have a masters degree, preferably in geography, landscape sciences, environmental studies, statistics or computer science. The candidate must be proficient in the Windows environment. Experience with S-PLUS/R, databases, XML, and web scripting e.g. HTML, asp/jsp, is a plus. The Landscape Information Scientist will be part of an active, exciting and creative team working on environmental applications. Required Skills: ArcInfo/ArcView and/or S-PLUS/R/SAS Start Date: December 2008 Pay Range: Minimum $40,000; based on experience Benefits: Health, 401k, Vacation/Holiday Location: Research Triangle Park, NC Job Number: 1420-02-02 Contact Phone Number: (919) 572-9505 x22 Contact Fax Number: (919) 572-2626 ]]>

<![CDATA[My well-established client providing contract laboratory services is seeking to grow the depth and breadth of analytical services they are currently providing to their pharmaceutical and medical device clients. With their projected growth, they have created a new opportunity for a highly motivated business development professional in the pharmaceutical space (familiarity with contract pharmaceutical analytical laboratory services and the drug development process). Qualifications: Candidates must be extremely motivated to extend their current client base and identify new business areas. Must have excellent prospecting skills and be able to take the lead role at trade shows. Must be able to independently develop sales process improvements and will assist in developing/updating marketing materials. Although this would not be a supervisory position initially, depending on the background and experience level, this role may be responsible for 1-2 direct reports in the next few years. BS Chemistry or related preferred (alternatively, someone who has a strong understanding of analytical needs within the drug development process from preclinical through NDA commercial manufacturing). 2+ years business development experience (only those with direct selling experience within contract pharma development services will be considered). No relocation available. Candidates should be based preferably in the RTP, NC area. ]]>

<![CDATA[Our client in RTP, seeks a Business Developement Manager to join their team. This is a direct hire opportunity with our client. Full benefits would be offered. The Health Sciences unit is the focus of the client's activities in contract and research services for early stage drug development and product safety assessment. We carry out projects for pharmaceutical, biotechnology and chemical companies to evaluate the safety and efficacy of new products. As the leading local provider of pre-clinical drug development support we are closely involved with helping many of North Carolina’s biotechnology companies understand the efficacy of their new drug leads by setting up animal models to profile the effects of the compounds. The Manager of Business Development is responsible for commercial sales, marketing and business development activities within the client's Health Science’s unit. This includes preparing annual sales goals and budgets, managing account executives and the client services department, developing and managing our larger accounts, leading sales activities targeted on the biotech and pharmaceutical industry, and leading the development of effective CRO business development practices. Services provided by Health Sciences include toxicology, DMPK, analytical chemistry, Bioanalytical services, and support for early stage drug development. The Manager of Business Development will work with our senior scientific staff to formulate and meet our sales goals. This will include identifying and meeting with target clients, tracking new business development activities, developing relationships with new and existing customers, representing RTI at professional and business development events. Qualifications: • MBA (PhD preferred) • Scientific or business experience in at least one of the unit’s primary service areas. • Five plus years experience in sales, account management within a Contract Research Organization environment. • Understanding of FDA’s or EPA’s requirements concerning product safety evaluation and the types of studies required for FDA/EPA product registration. ]]>

<![CDATA[3 Specimen Allocators needed November 18th - November 21st. The assignment may run as long as the 26th of November so interested applicants must have availability to work until the 26th. This project would be working with a large non profit in RTP. Specimen Allocators will work in a laboratory setting, with protection, pouring and sorting of urine samples to be sent out to these drug testing facilities. Candidates must be dependable and have availability for all days of the project. The hours for this project are 8am-5pm and the pay-rate will be $9/hour. Please send resumes to jennifer@greeneresources.com. Published Description: ]]>

<![CDATA[Clinical Trials Supplies Associate – Pharma Our client, a rapidly-expanding pharmaceutical firm headquartered in RTP, is actively recruiting for a very bright, skilled and knowledgeable professional for key role on its growing team. Company has many marketed products and many more in development. This will be an important role in bridging the clinical manufacturing and clinical research groups. Seek top-of-the-class industry professional with background in Clinical Trial Supplies/Materials to handle the day-to-day coordination of this function. Specific duties will include: • Process, track and maintain Study Product Requests, Purchase Orders, Invoices, etc. • Support Clinical Trial Supplies functions including monitor and maintain Clinical Trial Supplies SharePoint internet location (clinical trial supplies manufacturing, packaging and labeling status), shipment requests, protocol development, retrieve Project status information from project team members, issue and track departmental purchase requisitions. • Support/perform submission of proposal request, submission and approval activities. • Assist in preparation of SOPs, working processes, flow charts, logs, templates, check lists, training materials, databases, files and labeling. • Assist in providing written input on clinical trial supply issues to regulatory agencies. Selected candidate will combine excellent organizational and detail skills with knowledge of the clinical supplies/materials process and related documentation (usage of an electronic filing system important). Additionally, seek candidate who offers familiarity with both pharmaceutical manufacturing (cGMP) and clinical research – to support ability to collaborate with both groups. This is a highly dynamic and empowered setting. Demonstrated ability to autonomously and favorably coordinate the day-to-day responsibilities will be critical. This is a newly-created role due to growth and expansion. Seek a hardworking, disciplined and accomplished overachiever who will bring value. This position will begin as a contract and company will pay top dollar to attract top-notch candidate. ]]>

<![CDATA[Need help solving fluid mechanics problems for homework for school on weekly basis until the end of semester. I'm really busy with a lot of ventures right now outside of school, and just do not have time to figure out how to do this. Will pay good $$$. Compensation is negotiable. $50/problem-$200/assignment. This is not a full time job, I know, but nevertheless can be a good part time income of few hundred bucks per week for few hours of work in spare time. Please contact me immidiately for help.]]>

<![CDATA[Dependable laboratory technician needed part-time nightshift, 3PM to 11PM, in used oil analysis production lab. Minimum High School diploma needed, but lab and college science experience is preferred. Duties include sample preparation, manual testing, and minor programming and maintenance of automated testing equipment. Constant workload, so production mindset and attention to detail is a must. 20 to 30 hours per week required, perfect job for daytime college student. Possible full-time employment available after training.]]>

<![CDATA[Looking for individual with strong protein purification background. Maintain cleanroom facility and equipment. Revise and initiate GMP documentatins such as Batch Production Records, SOP's and Solution Records. Prepare media and buffers. ]]>

<![CDATA[The Animal Research Technician under general supervision performs daily, weekly, and monthly general duties associated with the position. Responsibilities include animal handling, animal husbandry, and data collection and recording, data package preparation, sample preparation, dosing, and surgical assistance. This position supports the research programs of the faculty by providing all services associated with the care and use of laboratory animals, daily care and monitoring of the health of all species; the Animal Research Technician is responsible for the daily care of animals in accordance with applicable laws and regulations, may serve as a lead/primary technician for an assigned project area and is technically skilled to perform various diagnostic or rodent colony management duties; in addition to the routine husbandry tasks (changing cages and racks, delivering food and water in accordance to established procedures, maintaining equipment and animal housing areas according to standard operating procedures and federal and state regulations), the incumbent may provide training to new employees/transfers, or technical assistance to Animal Facility Technicians. The incumbent participates in various projects as assigned and performs record keeping duties in a GLP environment. The incumbent will participate in holiday and weekend duty rotation for animal care , husbandry and study tasks . The Animal Research Technician works with minimal supervision and may be rotated to various locations to provide technical or back-up assistance on an as needed basis; and perform other duties as assigned. This position requires technical and procedural knowledge of all forms of administration tasks (SQ, IM, ID, IV, oral gavage, dermal, clinical observations, food consumption, body weights, necropsy activities). Excellent communication skills are needed as this position works closely with other technicians, scientists, veterinarians, and regulatory affairs. Prior animal research, animal husbandry, and/or animal laboratory experience is preferred. Additionally, excellent communication skills are needed as this position works closely with other technicians, scientists, veterinarians, and QAU. A BS or AA degree in Life Sciences and certification by the American Association for Laboratory Animal Science (AALAS) at the Assistant Laboratory Animal Technician (ALAT) level is preferred. Local candidates only please. No relocation assistance is available. Candidates must be able to lift at least 50lbs. For immediate consideration send your resume in word format]]>

<![CDATA[PURPOSE To formulate raw materials into finished bulk by following specific Batch Manufacturing Procedures (BMPfs). To ensure that the bulk product meets all Quality specifications and is produced in a timely manner based on the production plan/schedule. ESSENTIAL JOB FUNCTIONS 1. Apply all learned knowledge from Compounder 1 level and apply in everyday processes. 2. Provide training on batching processes/procedures to new employees as needed. 3. Must be able to work with little supervision and assist Compounder I and new employees when needed. 4. Set up and start all batching vessels and check all controls for adherence to Batch Manufacturing Procedures (BMPfs) procedures. 5. Capable of troubleshooting mixing/processing issues and provide analysis to Processing Engineers and R&D regarding batch issues/problems. 6. Maintain a safe and clean working environment at all times. ADDITIONAL RESPONSIBILITIES 1. Adhere to all Good Manufacturing Practices (GMPfs), Good Housekeeping Practices (GHPfs), and all safety regulations. 2. Assist other department personnel whenever needed. 3. Observe problems with equipment, raw materials, componentry or bulk product and alert Compounding Supervisor or Compounding Manager immediately. 4. Perform other duties as assigned by the Compounding Manager or by the Compounding Supervisor. MINIMUM RECRUITMENT STANDARDS 1. BS degree preferably in Chemistry or Food Science. Education can be substituted with two to four years job-related work experience in a compounding/formulating manufacturing environment. 2. Ability to work through multiple tasks simultaneously, manage time efficiently, and work with minimal supervision is required. 3. Ability to lift and move up to 50 pounds is required. 4. Demonstrated ability in analytical reasoning skills is required. 5. Good basic math skills and the ability to convert between metric and English measurement systems (lbs ¨ kg ¨ g). 6. Maintain excellent team working relationships. 7. Must have good verbal communication skills, good interpersonal skills, and attention to detail. Please send resume to raleigh@pridestaff.com]]>

<![CDATA[Life Sciences Business Analyst (Job Code: dw1021) d-Wise is a growing technical consulting company based in Raleigh, NC which delivers custom software solutions in the life sciences industry. d-Wise works with customers to develop data warehousing and business intelligence solutions to solve their business problems. d-Wise has formed a life sciences practice to support the development of custom solutions for pharmaceutical and biotechnology companies with a focus on helping customers leverage industry standards, support technology integrations, define business processes, and deliver SAS solutions. d-Wise is recruiting a Life Sciences Business Analyst who will be responsible for implementing solutions within pharmaceutical and biotechnology companies with a focus on data integration and standardization. As part of a rapidly growing consulting company, this position provides a motivated individual the opportunity for significant growth. Responsibilities will include: • Working with customers to define requirements using interviews, requirements workshops, business analysis, task and workflow analysis around technology solutions in the drug development process • Ensuring customer relationships are properly managed throughout the development/implementation of the solution • Proactively communicate and collaborate with external and internal customers to analyze information needs and functional requirements and deliver the following artifacts as needed: Business requirements, Functional Specifications, Use Cases, and associated project management documentation • Interacting with multiple levels of an organization including executives, managers, and domain experts. • Be the liaison between the customer and the d-Wise technology teams • Travel to customer sites for meetings and/or project work as needed. This may include international travel Skills and Experience • Minimum 5 years experience within the drug development process and 2 years experience in a project management role preferably on technology projects • Excellent verbal and written communication skills and the ability to interact professionally with a diverse customer group • Knowledge of relational databases, integrating data, and data warehousing techniques • Experience with software development including requirements gathering, design, development and validation • Knowledge with industry standards including CDISC and HL7 standards • Ability to work on multiple projects, set priorities and work independently • Experience with SAS solutions including SAS Data Integration, SAS Drug Development, and SAS Business Intelligence is preferred but not required Benefits: • Full Medical Benefits • 401-K with company matching and Profit Sharing Plan • Ability to become an integral part of a rapidly growing company Please send your resume and cover letter to jobs@d-wise.com and include the job code (dw1021) in the subject line of your email. ]]>

<![CDATA[ Opus Scientific is currently looking for a formulations chemist for a 6 month contract opportunity in Research Triangle Park, NC.   This position may go permanent for the right candidate.     Responsibilities: ·         Prepare developmental pesticide formulations ·         Perform a variety of analytical and physical tests. ·         Record and analyze test data obtained and prepare detailed reports on the observations and determinations made. ·         Assists in the modification and preparation of test procedures, instructions, and the training of laboratory personnel.   Requirements ·         AAS Degree in Chemistry or related field with a minimum of 2 years of relevant chemistry laboratory experience. ·         1 year - Preparation: Weighing, blending/mixing, wet and dry milling, coating, extrusion; Analysis: rheometry, titration, colorimetry, particle size analysis, physical chemical testing of liquid as well as dry formulated products. ·         Minimum Experience - 1-year laboratory bench experience in synthesis, formulation, preparation   Desired: ·         BS Degree in Chemistry with minimum of 1 year relevant chemistry laboratory experience in the formulation of pesticides. ·         Specific ability to carry out analytical procedures such as rheometry, particle size analysis, light microscopy. ·         Strong skills in MS Excel and skilled in Lotus Notes.   Compensation: ·         $16 - $17/hour, depending on experience and education   Job Location: ·         Research Triangle Park, NC   Contact: For more information send your resume to Greg at <a href="mailto:jobs@opusscientific.com" rel="nofollow">jobs@opusscientific.com</a>.  Please include the title of the job "Formulations Chemist" in the subject line of the email.]]>

<![CDATA[Are you looking for an Excellent opportunity with a biotech company? Supported executive level officer of a corporation for a minimum of 3-5 years. Experience in staffing and supporting an expanding location, prior office management, safety and security spport to a facility a plus. Expert in Microsoft Word, Excel and PowerPoint, flexible hours, travel arrangements and expense reports (domestic and international), strong oral and written communication skills. This position is located in RTP. The hours are M-F and weekends (you need to be flexible). The salary is $50/yr plus. You must have a clean criminal background, able to pass a drug test, and able to start asap. Anyone needing to give a two weeks or one notice need not apply. ]]>

<![CDATA[ Opus Scientific has an opportunity for Candidates with a Background in Biology in North Carolina!   Opus Scientific is in need of an Assistant Lab Technician in Research Triangle Park (RTP) who can use his or her experience from biology class.   This position is entry-level allowing you to gain valuable experience in a Fortune 100 chemical company!   MUST be available both Weekdays and Weekends    Responsibilities: ·        Evaluate efficacy of seed treatment materials ·        Prepare and maintain seed and plant materials for lab, greenhouse, and field tests ·        Assist in chemical application of seeds and aid with recording and processing of data   Requirements: ·         Previous experience in working in laboratory setting ·         High school diploma with biology course   Compensation: ·        $12 - $16 /hour   Job Location: ·         Research Triangle Park (RTP), NC   Contact: For more information send your resume and cover letter to Greg at jobs@OpusScientific.com. Please write the title of the job “Assistant Lab Technician" in the subject line of the email for rapid processing.   Keywords: Chemistry, chemist, analytical chemistry, medicinal chemistry, chemical manufacturing, biology, agriculture, lab, technician, cGMP, label, labeling]]>

<![CDATA[ Opus Scientific has an opportunity for Candidates with a Background in Chemistry in North Carolina!   Opus Scientific is in need of an Assistant Chemist in Research Triangle Park (RTP) who can use his or her experience from chemistry class.   This position is entry-level allowing you to gain valuable experience in a Fortune 100 chemical company!   Responsibilities: ·        Conducting method development and residue analysis   Requirements: ·        BS in Chemistry or Biochemistry or related fields ·       Proficiency in the fundamental aspects of experimental lab and data analysis   Desired Skills: ·         Experience with wet chemistry, LC/MS/MS and GC/MS for quantitative analysis ·         Familiarity with Good Laboratory Practices (GLP)   Compensation: ·        $13 - $14.50 /hour   Job Location: ·         Research Triangle Park (RTP), NC   Contact: For more information send your resume and cover letter to Greg at jobs@OpusScientific.com. Please write the title of the job “Assistant Chemist “in the subject line of the email for rapid processing.   Keywords: Chemistry, chemist, analytical chemistry, medicinal chemistry, chemical manufacturing, biology, agriculture, lab, technician, cGMP  ]]>

<![CDATA[Manufacturing industry leader seeks top candidates for excellent opportunities! Are you a manufacturing professional looking for a long term opportunity with a stable company? If your answer is yes, we want to speak to you. We are currently seeking semiconductor operators. Qualified candidates will perform a variety of functions in the production of semiconductor devices such as wafer fabrication, assembly and testing. Primary responsibilities will include operating equipment, assisting in setting up workstations, and following written or verbal process specifications in completing all assignments. Requirements: Attention to detail, ability to work unsupervised, and demonstration of mechanical aptitude Highly motivated and willing to learn Ability to work 12-hour standing night shifts Criminal background check and drug screen High school diploma or equivalent Preferred Requirements: Microscope experience Technical skills Cleanroom experience Previous machine operation experience Positions typically require a minimum of 2 to 3 years of manufacturing experience. The pay range for these positions will be between $11.55-12.10/hour depending upon shift. Please apply online at www.creejobs.com for immediate consideration. ]]>

<![CDATA[If you have a BS in Chemistry or an equivalent degree and have had at least 1-2 years of hands-on, laboratory experience in GC/MS spectral interpretation, preferably in Semi-volatiles, we are interested in talking with you. An ideal candidate would be an experienced and qualified, production laboratory analyst, capable of analyzing environmental samples in various matrices on a GC and/or GC/MS instument. The ideal candidate will also have the ability to review and qualify the instrument output and provide written narratives concerning the data acceptability for submittal to our nationwide network of clients. An absolute must for this position would find the applicant fully capable of performing a comprehensive inspection and review of GC/MS Semi-volatile data packges in order to determine it's compliance and acceptibility in accordance with promulgated USEPA Contract Laboratory and SW-846 methodologies and any associated Statement(s) of Work. CompuChem is a pioneering leader in USEPA methods and has led the EPA Contract Laboratory Program in the number of environmental samples analzyed over the past 28 years. If you are capable of meeting the requirments indicated herein, please contact us if you are considering a change of pace and/or a new employment opportunity. We are an Equal Opportunity Employer (EOE) located at 501 Madison Avenue, Cary, North Carolina and have been in business since 1980. <a href="http://www.compuchemlabs.com" rel="nofollow">http://www.compuchemlabs.com</a>]]>

<![CDATA[Part-time position (20-25 hours per week) available to assist laboratory analysts in the processing and analysis of air quality samples. Although initially part-time the position is permanent with a likely potential to become full-time. Duties would include sample login and distribution, sample prep and general lab assistance. Upon obtaining full-time status, benefits would include health/dental insurance, 401k and more. Applicant must be well-organized and get along well in group situations. Please reply to set up interview appointments.]]>

<![CDATA[Currently recruiting for a Quality Control Manager (Chemistry / Stability ). This is currently the only Quality position that I am working on at the moment. Please email me directly at Dean.Hansen@DiscoverySolutionsLLC.com if you believe that you are the “ideal” candidate. I’m ways looking to increase my connections, so I will also accept any network invitations. If there is anything I can do for you please don’t hesitate to ask. This Company located in the RTP area of North Carolina applies its unique drug development capabilities and expertise to commercialize complex proteins and monoclonal antibodies that until now have been impossible or very expensive to develop through traditional means. Currently seeking a Quality Control Manager (Chemistry / Stability) The manager of the Quality Control Chemistry / Stability group will be responsible for oversight of the release and stability testing of GMP master plant banks and drug substance materials intended for use in the clinical setting. The manager level will be accountable for the review and approval of stability protocols and summary reports of Drug Substance materials, ensuring their compliance with ICH guidelines. The release and stability assays include: SDS-PAGE, rpHPLC, IEF, SEC, HIC, ELISA, Southerns and Westerns. This position is expected to spend at least 25% of the time in the QC laboratories assisting with equipment qualifications, assay trouble shooting, data generation and review. The manager will be responsible for the coordination of in-process, release and stability assays associated with GMP production. As products progress in the clinical setting, this position will be accountable for ensuring the qualification and subsequent validation of the equipment and methods in accordance with internal procedures and with FDA / international regulations. This person will be responsible for the management of all laboratory exceptions stemming from the Stability or Chemistry groups. The manager is expected to provide direct supervision to the Quality Control Chemistry and Stability staff. The ideal candidate will possess leadership experience in a GMP Quality Control Chemistry / Biochemistry laboratory. Qualifications • 5 to 8 years of experience in a cGMP Quality Control laboratory environment, preferably in the biotech industry. • An ideal candidate will possess previous experience in leadership role. • Technical Skills: ELISA, CPE, SDS-PAGE, IEF, Western, Southern, rpHPLC, SEC, Peptide Mapping, General Laboratory Testing (pH / Appearance / Osmolality / UV). • Software Skills: MS Outlook, MS Excel, MS Word, Empower, NWA, Quantity-One, Trackwise. • Education: A minimum of a Bachelor of Science: Chemistry / Biochemistry / Other Life Sciences Degrees ]]>

<![CDATA["b Requirements # Candidate must have an understanding of the consulting engineering space and have a proven track record of managing a division or company of more than 200 people. # Candidate must be a strategic thinker as well as tactical manager. Qualified candidate should understand developing strategy for markets and opportunities and implementation ability to see those long-range plans through. Ideal candidate will be a team leader. # Must assist Branch managers in development and maintenance of high quality professional services function. # Build a corporate culture based upon: honesty, trust, mentoring, new ideas, risk taking, giving credit, integrity, and selflessness. Key Components: Planning Business Development Human Resources Client Service Financial Profitability Team Leadership Experience: At least ten years of experience in the consulting engineering field, of which at least five years have been in a Senior Management capacity. Education: Bachelor's degree in Engineering Employee Type: Full-Time Employee Req'd Education: 4 Year Degree Base Pay: $100,000 - $120,000 /Year Job Application: www.EnvironmentalExpertRecruiter.com/Job137 for Expert Witness (you might have to copy and paste this address if your browser does not support it)." ]]>

<![CDATA[ Our client, a rapidly-expanding pharmaceutical firm headquartered in RTP, is actively recruiting for a very bright, skilled and knowledgeable professional for key role on its growing team. Company has many marketed products and many more in development. This will be an important role in bridging the clinical manufacturing and clinical research groups. Seek top-of-the-class industry professional with background in Clinical Trial Supplies/Materials to handle the day-to-day coordination of this function. Specific duties will include: • Process, track and maintain Study Product Requests, Purchase Orders, Invoices, etc. • Support Clinical Trial Supplies functions including monitor and maintain Clinical Trial Supplies SharePoint internet location (clinical trial supplies manufacturing, packaging and labeling status), shipment requests, protocol development, retrieve Project status information from project team members, issue and track departmental purchase requisitions. • Support/perform submission of proposal request, submission and approval activities. • Assist in preparation of SOPs, working processes, flow charts, logs, templates, check lists, training materials, databases, files and labeling. • Assist in providing written input on clinical trial supply issues to regulatory agencies. Selected candidate will combine excellent organizational and detail skills with knowledge of the clinical supplies/materials process and related documentation (usage of an electronic filing system important). Additionally, seek candidate who offers familiarity with both pharmaceutical manufacturing (cGMP) and clinical research – to support ability to collaborate with both groups. This is a highly dynamic and empowered setting. Demonstrated ability to autonomously and favorably coordinate the day-to-day responsibilities will be critical. This is a newly-created role due to growth and expansion. Seek a hardworking, disciplined and accomplished overachiever who will bring value. This position will begin as a contract and company will pay top dollar to attract top-notch candidate. Interested? Please email your resume for immediate consideration to DeniseD@frankelstaffing.com ]]>

<![CDATA[RTI is an independent organization dedicated to conducting innovative, multidisciplinary research that improves the human condition. With a worldwide staff of more than 4,000 people, RTI offers innovative research and development and a full spectrum of multidisciplinary services. Universities in North Carolina founded RTI in 1958 as the first scientific organization in and centerpiece of the Research Triangle Park. ** Please apply at www.rti.org/job11639 to be considered. Thank you ** RTI’s Center for Aerosol Technology is seeking a Materials Scientist for a position in the cement technologies laboratory at RTI’s main campus in Research Triangle Park. Responsibilities will include: • Fabricating cement slurries to specification • Developing hardware to place the cement • Testing the chemical, rheological, and mechanical properties of the cement • Writing reports • Developing intellectual property • Working closely with other laboratory personnel All operations of the laboratory will be conducted in accordance with RTI’s laboratory safety guidelines. Qualifications: • B.S./M.S. in Mechanical or Civil Engineering, Chemistry, Materials Science or related field. • Strong analytical and creative problem-solving with sound working knowledge of cement chemistry, mechanical and/or civil engineering, cement analysis tools, and cement rheology. Experience with basic instrumentation for measuring cement properties a plus. • Highly interactive interpersonal skills for effective communication with project team members and various staff (including engineers, scientists, technicians, clients, vendors, etc). • Demonstrated verbal and written communication skills to successfully follow instructions outlined in experimental test plans, request clarification from the project manager, and work equally well independently and as part of a larger team. • Self-motivation and a strong attention to detail are required to efficiently complete tasks outlined in experimental test plans on schedule. • Familiarity with laboratory documentation procedures and quality assurance concepts. • Creative ability to solve problems that arise without compromising data quality. • Ability to use Excel and Word to prepare graphs and tables for reports. A basic understanding of statistics is a plus. • Aptitude with tools and mechanical devices. Some projects will require physical effort (e.g., working from a 15 foot ladder or carrying lbs of equipment). • Must be a U.S. Citizen. Equal Employment Opportunity We are proud to be an EEO/AA employer M/F/D/V ** Please apply at www.rti.org/job11639 to be considered. Thank you ** ]]>

<![CDATA[Title: Senior Study Director Location: Baltimore, MD Salary: Open, Depending on Experience Hours: Standard Business Terms: Full Time/Permanent Responsibilities and Duties •Interact with clients in the definition of study protocols and development of SOWs •Revise and implement scientific study protocols and SOPs •Design and supervise in vitro biochemical drug metabolism and in vitro toxicology studies, interpret results, and write reports •Lead, train, and supervise Study Director •Motivate and lead technical staff; complete performance reviews •Manage department capital and operating budget vs. studies •Hire additional technical staff when appropriate •Participate with Director in the development of new business •Maintain GLP status of laboratories and studies •Participate with Sales force in the development and publication of assays offered Qualifications/Skills and Knowledge Requirements •Ph.D. in pharmacology, ADME, toxicology, biochemistry, medicinal chemistry, pharmaceutics, or related discipline •Minimum of 5-7 years designing, interpreting and reporting drug metabolism and in vitro toxicology studies •CRO Study Director experience preferred but not required •Demonstrated experience in the direct supervision of Ph.D. and B.S./M.S. lab staff Critical Skills •In-depth knowledge of enzyme kinetics, bioanalytical methods development and validation, and structure elucidation using MS/MS techniques •Prioritizes and manages multiple conflicting projects simultaneously without compromising quality •Communicates clearly with staff, management, and external clients. •Demonstrates calm, fair, and balanced resolution of personnel issues •Excellent written and oral communication skills •Excellent track record of publications in peer-reviewed journals ]]>

<![CDATA[Full or Part-time position available for a GLP Quality Assurance auditor. Position requires at least 2 years GLP auditing experience and a strong ability to adapt to an unconventional and innovative research environment. Responsibilities include but are not limited to auditing and assisting with the assurance of compliance to FDA and OECD GLP guidelines and providing administrative/organizational assistance to corporate management as needed. Educational background or professional certification is not a consideration for this position. However, demonstrated professionalism with excellent written and verbal communication skills and a willingness to learn are a must. ]]>

<![CDATA[General Summary: This position is responsible for the operation of the Quality Assurance Unit and the management of personnel within the unit. The incumbent is responsible for planning and coordinating the activities necessary to provide management with confidence that the Institute?s products and services satisfy quality and regulatory requirements and for reporting the status of such compliance to management on a periodic basis. Key Responsibilities: - Manages the Institute?s quality assurance unit and its personnel, including the establishment of goals, schedules, priorities, staffing, training, and budgets. - Reviews quality assurance unit system and methods on a periodic basis to ensure its efficient operation and its compliance with applicable regulations and standards. - Reviews and disseminates regulatory reference information that may affect the operation of the quality assurance unit or other areas. Position Specific: - Reports the status of compliance with applicable regulations and standards that relate to studies, operations, and facilities to management. - Reviews quality assurance unit inspection reports to assess findings, responses, and need for follow-up activities. - Ensures that the Good Laboratory Practice Master Schedule is maintained according to regulations, standards, and procedures. - Serves as a key contact for regulatory inspections and provides input for responses to those regulatory inspections. - Provides project costing estimates and quality assurance unit input for proposals. - Serves as an internal consultant for system validation projects. - Performs audits of subcontractors who provide support for regulated work. - Effectively communicates with Institute personnel, clients, subcontractors, regulatory inspectors, and third party organizations. - Hires, reviews, motivates, and disciplines, as appropriate, quality assurance unit personnel. - Ensures that budgets are realistically established and attained. Requirements/Minimum Qualifications: - Bachelor?s degree in relevant discipline - 8-10 years of experience with regulations and standards (i.e., Good Laboratory Practices) - Previous background/experience implementing GLP - Previous training and quality systems development experience - Ability to lead, motivate and discipline staff - Ability to successfully implement business processes - Ability to observe appropriate safety and study requirements by reading, understanding and following Standard Operating - - Procedures (SOP), Good Laboratory Practice (GLP) requirements and study protocols. - Certification as a GLP Professional (e.g. RQAP-GLP) is preferred. Apply online at <a href="http://www.southernresearch.org" rel="nofollow">http://www.southernresearch.org</a> or <a href="http://careers.peoplecapital.com/sricareers/details.asp?jid=11091&p=2" rel="nofollow">http://careers.peoplecapital.com/sricareers/details.asp?jid=11091&p=2</a>]]>

<![CDATA[RTI International, the nation’s second largest independent, nonprofit scientific research organization is seeking an entry level statistician for its Research Triangle Park campus. More than 120 statisticians comprise the Statistics and Epidemiology Unit and is one of the largest and most comprehensive in private industry. Our statisticians conduct cutting-edge research in survey and sample design, modeling, and statistical analysis. A Statistician 1 will work in a variety of fields, including international health, governance, and education, as well as health services, economic and social development, education and training and the environment. The Statistician 1 position requires the ability to work independently and as a member of a team to deliver high quality work. Eighty to ninety percent of daily work is at a computer; the remainder would be in project planning meetings and conference calls. Opportunities also exist for writing proposals and reports. Responsibilities: • Apply standard statistical and/or data management software package(s) to execute data processing, and data analysis activities • Conduct routine/established data processing and data analysis under supervision • Assist in the preparation of research proposals by providing computer programming support, literature reviews and effective bio-sketches • Carry out appropriate professional development efforts Qualifications: • Candidate must have experience with SAS and Excel. (Sample of SAS code required) • Demonstrated data manipulation and data management skills. • Bachelor’s degree in Statistics, Biostatistics, Biomathematics, or Mathematics and one year or less experience. • Excellent written communication skills as evidenced in the cover letter ***For more information and to apply, please visit www.rti.org/careers and refer to: Statistician 1 (Job ID 11127)*** We are proud to be an EEO/AA employer M/F/D/V ]]>

<![CDATA[Successfull applicant will help assist with day to day operation of a small environmental/aquatic management company. Tasks can be strenuous, (much like landscaping at times) and in challenging (wet) conditions. Applicants must be able to lift 50#s, be a hard worker and have a positive attitude. Must have a desire and interest in maintaining and improving water quality in streams, rivers and other water ways. Good computer skills, experience with heavy and small equipment (excavator, bobcats, mowers, trucks and trailers) a plus. Ideal candidate will have a desire to learn and grow with the business. Submit resume and any question. Looking for 10-20 hours until summer, where we expect you to go full time through summer. Ideal for college students looking for field experience and future employment opportunity. The right employee will be offered a full time position after graduation from college. We look forward to having you on our team.]]>

<![CDATA[Our company, located in the Research Triangle Park area of NC, is developing a new high performance micro-concentrator solar cell array that can be produced at a fraction of the cost compared to alternative technologies. Because of the low cost parallel processing approach coupled with the high performance optics and multi-junction solar cell combination, the solar module will have the lowest $/W ratio available in the marketplace. Solar Cell Technician Background: The solar industry is growing at an unprecedented rate and is demanding the highest performance solar modules at the lowest possible cost. Our company has developed unique technology licensed from the University of Illinois which is capable of massively parallel transfer printing small solar cell chips onto a solar panel at very low cost. The technology enables the use of very high performance multi-junction III-V compound semiconductor solar cells. Responsibilities: The Solar Cell Technician will be responsible for assisting other engineers in the development of high concentration photovoltaic solar cells and modules. The candidate will also be responsible for testing and characterizing prototype solar cells and modules. The candidate will work with a dynamic team of engineers and partners engaged in this exciting and multi-disciplinary field and will report directly to the VP of Technology. Qualifications: Candidate must have an Associates, BA, or BS degree and 3+ years of industry experience. The individual must be flexible, eager to learn, and hard working. Experience with optoelectronics, microelectronics, and/or solar technology is highly desirable. In addition, the candidate must be a highly motivated individual with excellent verbal and written communication skills and who is a good team player. To Apply: To respond to this opportunity, please go to: <a href="https://administaff.ats.hrsmart.com/cgi-bin/a/highlightjob.cgi?jobid=46501" rel="nofollow">https://administaff.ats.hrsmart.com/cgi-bin/a/highlightjob.cgi?jobid=46501</a> EOE ]]>

<![CDATA[Are you looking for an EXCELLENT PART TIME Customer Service Rep opportunity for a biomedical company? A local Biomedical company in Durham, NC is currently in need of a stellar Spanish Speaking Customer Service Rep. The hours Hours are SATURDAY-TUESDAY 5:15a-3p. The employee will be on a daily basis video monitoring participates for a site study and placing outbound calls to particiates and recording data. Attention to detail is a must. Good Customer Service skills are required. Light Data Entry and Typing are involved in the documentation of the participate. Two years of call center experience in relative field is required. Candidate Profile *2 years experience in relative field. *Attention to detail, multi tasker, flexible and reliable. Candidate Skills *2 years experience in a call center environment. *Fluent in Spanish and English *Excellent Customer Service phone communication skills. *A clear criminal background record. ]]>

<![CDATA[Marine Air Ground Task Force (MAGTF) Science & Technology Analyst Camp LeJeune, NC Shee Atiká Technologies is an Alaska Native Corporation SBA 8(a) Enterprise and veteran owned small disadvantaged business that provides products and services for the aerospace and defense industries. We provide an array of engineering, technical support services, resource planning and management services for these specific industries. Our goal is to provide our clients with actionable solutions to their engineering, technical and management challenges. Currently, SAT has an opening for a Marine Air Ground Task Force (MAGTF) Science & Technology Analyst at our Camp LeJeune, NC location. This position is full time and full benefits are provided including medical, dental, vision, life insurance, short- and long-term disability insurance and 401(k) plan. Duties and Responsibilities: The analyst will work as a member of the II Marine Expeditionary Force G-9 Science, Technology and Innovation Staff. Duties will require the research and review of appropriate source materials, investigate potential material and non-material solutions, conduct interviews, participate in information and planning meetings and conferences; liaison with government and non-government organizations and industry; and provide periodic briefings and reports as it supports the following tasks:  Analytical, technology and engineering support services  Research support services  Liaison services  Support to UNS/UUNS/JOUNS processes  Project management support Requirements:  Broad USMC experience in MAGTF operations.  Demonstrated proficiency with Microsoft Office software.  Demonstrated verbal and written communication skills along with the ability to operate in a fast paced military office environment.  Secret Clearance Preferences:  Former Marine Officer or Senior Enlisted.  Recent combat experience in OIF or OEF. To apply for this position, please use the following URL: <a href="http://tbe.taleo.net/NA7/ats/careers/requisition.jsp?org=CORSAIR&cws=4&rid=54" rel="nofollow">http://tbe.taleo.net/NA7/ats/careers/requisition.jsp?org=CORSAIR&cws=4&rid=54</a> or send your resume to Margot Washington at margot@kirklandoffice.com]]>

<![CDATA[My client, a local leader in web-based instructional tools, is actively recruiting for Top-Notch recent grads with degrees in math, chemistry and/or physics, to work on projects related to technology-based teaching and testing. This company is developing cutting-edge tools and is growing rapidly. Seek very sharp and quality-driven professionals to contribute in course/textbook development. Potential for long term growth opportunities with excellent benefits package and flexible schedules. The primary function is to develop textbook questions/answers to be used by the customer base. To successfully do so, candidate must have excellent knowledge of the subject area (math chemistry, and/or physics) as well as some programming knowledge (company uses PERL but will train), HTML exposure and excellent verbal and written communicative skills. Candidate will be writing answer algorithms and any experience in a similar role will reduce the learning curve. Finally, seek candidate with sincere interest in learning and development. This is an education-driven client base and best candidates will have a commitment to the mission. BS (or higher) degree in math, chemistry, or physics is a Must. Knowledge of html, Perl, or other programming/coding languages necessary. Client will consider temp-to-permanent or contract candidates. Interested? Please email your resume (as a word or txt file), for immediate consideration to DeniseD@frankelstaffing.com. Thanks! ]]>

<![CDATA[Seeking a temporary Research Technician to work for a UNC-Chapel Hill department. Must have experience using Taqman real-time PCR with RNA. FT/PT flexible schedule: minimum 4 hours a day up to 40 hours a week within the hours of 8am-5pm, Monday - Friday. This position will last for a period of 4 to 6 weeks. Pay for this position is $20/h. If you have this experience and are interested in applying please visit <a href="http://hr.unc.edu/tht" rel="nofollow">http://hr.unc.edu/tht</a> and call (919) 962-2900 for more information.]]>

<![CDATA[If you have a Ph.D. or MS degree and significant years of pharmaceutical industry experience in the formulation development of DPI/MDI and other pulmonary and nasal products as well as some supervisory experience, then please submit your resume. This position is not based in NC and will require relocation. Low cost of living and attractive area of Midwest. Position title will vary depending on the level of experience, but can be anywhere from Sr. Scientist to Associate Director. ]]>

<![CDATA[The company is seeking a high talent, creative individual who can bring market insights, technical expertise and communication skills to a Business Development role focused at discovering and developing wholly new products and opportunities in the area of Clinical and Infant Nutrition. Primary Role: Manage existing portfolio of products/customers in market segment and expand portfolio/customer base with profitable/sustainable top line growth to meet/exceed strategic plan projections. Refine and lead plan execution and functional team to grow the CIN and Pharma business in North America beyond the current base business with profitable specialty products. Specifically: Build a comprehensive business plan for CIN North America. Identify and adapt value propositions for the North American market, primarily in the Clinical and Infant Nutrition segment, addressing current and unmet market needs. Use internal and external experts to build National Starch Food Innovation’s image and credibility in the CIN and Pharmaceutical market space. Working in conjunction with the current customer facing organization, contribute product knowledge and industry expertise to develop short to long term projects and opportunities. Manage issues regarding the current product/customer portfolio and the small team dedicated to this area. Over time, expand into Pan Atlantic collaboration and communication. Interface cross functionally internally, with customers and with partners. Minimum of 5-7 years experience that includes organizing and leading cross-functional teams and project management of complex multi dimensional projects. Technical background. Technical aptitude. Industry experience/insights related to Clinical or Infant Nutrition. Marketing experience a plus. Strong communication skills, demonstrated internally and externally. Track record of innovative thinking, interpersonal effectiveness, successfully dealing with ambiguity, driving for results. Bachelor’s degree in technical area required. MBA a plus. Please send in-depth cover letter outlining experience with your CV/Resume for consideration. ]]>

<![CDATA[<a href="http://www.healthdec.com" rel="nofollow"><img src="http://www.healthdec.com/images/hd_logo.gif"></a> <img src="http://www.healthdec.com/images/hd4u/HD4U_green_cham.jpg"> Head of Clinical Affairs <hr align="center" size="2"> Highly visible top leadership position with a progressive, growing Clinical Research Organization in Durham, NC.  We are looking for a leader with the depth and experience to inspire, motivate, and build a global best-in-class clinical organization.  You must be effective at managing up and down the organization and leading by example.  You will be leading senior clinical staff and working with the executive team to position the department and company for aggressive growth and global expansion.  This is a unique opportunity to work with extremely talented individuals in a highly innovative company to shape future direction and lead a large department through an exciting transition. Our approach to clinical trials is robust, tested, and technology driven with the consistent results of shaving 10 to 25% off timelines.  We want a dynamic person that has an agile mind and is creative, strategic, and looking for challenge in growing our clinical team to global excellence. We are looking for an effective leader with 10+ years leading global clinical research teams, with the ability to effectively provide strong management across Monitoring and Project Management.  You must be a leader among leaders, with an inspiring yet resolved approach.   Responsibilities: ·         Work with the Executive Committee to provide strategic corporate and departmental planning needed to facilitate global expansion and the building of robust Project Management and Clinical Affairs infrastructure to support rapid growth and a geographically diverse work force. ·         Develop business opportunities by providing leads, nurturing current and prospective clients, attending bid defenses and undertaking marketing activities such as industry presentations, article authorship, etc.  Share opinions and expertise on marketing and business development strategies, proposal content and approach, presentation content, etc. ·         Serve as strategic consultant to clients – advise on drug development programs, protocol design, regulatory strategy, etc. ·         Share knowledge and clinical research project management expertise with growing project management team ·         Ensure that the operational aspects of the department including budget, resources, employee development, quality deliverables and vendors are being met and that suitable performance standards are in place.  Develop strategy for scaling operational aspects for aggressive growth and global expansion. Qualifications: ·         10+ years of relevant clinical trial experience; experience in a global team environment required ·         5+ years management experience working with project management teams ·         Demonstrated success in leading 50-150 person department through high growth, preferably a transition from a small to mid-size CRO.  Experience building infrastructure, policy, SOPs and other processes ·         Experience in forming and managing global alliances.  Experiences with global acquisitions and managing integration ·         Experience managing a remote employee workforce ·         Experience with drug development strategies to serve as strategic consultant to clients ·         Advanced customer service skills and experience contributing to business development activities – client satisfaction, proposal preparation, bid defenses, etc ·         Ability to understand, embrace and improve new technologies ·         Problem solver that proactively identifies and resolves issues using creative approaches ·         Able to envision, design and implement solutions that integrate business needs with flexibility ·         Strong background in project management and monitoring.  ·         Able to work with a variety of internal/external customers at every level ·         Knowledge of Data Management and Biostatistical principles are a plus.   Health Decisions offers a casual environment working with exceptional professionals, competitive compensation, and countless opportunities for growth and learning. Health Decisions is an Equal Opportunity Employer (EOE). To learn more about Health Decisions, please visit our website: <a href="http://www.healthdec.com" rel="nofollow">www.healthdec.com</a> Interested candidates should send their resume, cover letter, and salary requirements to <a href="mailto:careers@healthdec.com" rel="nofollow">careers@healthdec.com</a> .  Please reference the position title in your subject line. ]]>

<![CDATA[Must have DOCUMENTUM administrator experience. Full time position with biotech company in RTP, NC. Will be responsible for administration of DOCUMENTUM clinical content management system. If you do not have experience with DOCUMENTUM please do not apply. ]]>

<![CDATA[Performs product manufacturing and provides manufacturing support for a large company in the RTP area. Individual will perform inoculum expansion, recovery and purification according to SOPs and instruction contained in MPRs. Will also work with raw materials intermediates, labware and prepare buffers and solutions for GMP manufacturing. ]]>