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<![CDATA[The Division of Sleep Medicine at Brigham and Women’s Hospital is looking for participants for a research study about how light affects sleep. The study involves a 3 week screening process and then 14 days living in our facility. We are looking for people who are: - Healthy - Non-smokers - Aged 18-30 Receive up to $2,910. Interested? (617)525-8799 lightstudy@partners.org ]]>

<![CDATA[Participants needed for 9-10 Day Sleep Research Study on the effects of light on sleep at Brigham and Women's Hospital *Must be 18-30 years old *Not on any medications RECEIVE UP TO $2,150 Contact Us at (617) 732-4311 light@rics.bwh.harvard.edu ]]>

<![CDATA[PHYSICIAN BILLING COMPANY SEEKING PROFESSIONAL INDIVIDUAL TO HANDLE INSURANCE COMPANY CLAIMS FOLLOW-UP AND APPEAL OF DENIED CLAIMS AND INEQUITABLE REIMBURSEMENTS. RESPONBILITIES ALSO INCLUDE DATA ENTRY OF PHYSICIAN CHARGES AND REVENUE. Requirements FAMILIARITY WITH MEDICAL MANAGER PHYSICIAN BILLING SOFTWARE PREFERRED. TELEPHONE ETIQUETTE REQUIRED. EXCELLENT KEYBOARDING SKILLS. ACCURACY AND ATTENTION TO DETAIL REQUIRED. GOOD COMMUNICATION SKILLS AND PROFICIENCY IN MICROSOFT WORD AND EXCEL. BACHELOR'S DEGREE IN BUSINESS ADMINISTRATION/ HEALTH CARE SERVICES ADMINISTRATION PREFERRED. SALARY COMMENSURATE WITH EXPERIENCE. EXCELLENT BENEFIT PACKAGE. Job Application: <a href="http://MedicalBillingStaffing.com/Job434" rel="nofollow">Apply Here</a> for ""Medical Billing"". Base Pay: $30,000 - $37,500 /Year Employee Type: Full-Time Employee Education: High School ]]>

<![CDATA[General Function: Supports the development of or writes various technical documents: requirements, specifications, test plans, and user manuals. Understands validation concepts in order to produce documentation for validated systems. This level contractor will provide technical writing under the guidance of a Project manager and/or Team lead. Duties may include: * the development of technical documents; requirements; specifications; test plans and end user manuals. This level contractor will write technical documentation under FDA guidelines including IQ; OQ and PQ along with 21 CFR 11. Location: Cambridge, MA Duration: 6 months Rate Target: $40 to $50 W2 DOE **** Third party resumes will not be accepted!**** If you have interest in this position, please contact me immediately. GTT has over 8 years of experience in IT consulting, including staff augmentation and project engagements. We offer health insurance, 401K, and disability insurance to W2 employees. Also, we will contract on a Corp to Corp basis. Please send Word version of resume to biotechjobs@grouptechinc.com and reference this ad when applying. ]]>

<![CDATA[Elite Egg Donation Agency Seeks Sophisticated Donors • A DISTINGUISHED AND WELL-REGARDED AGENCY: We are recognized by physicians through-out the North East as a leader in collaborative reproduction. Physicians specializing in fertility recommend that their patients work with our agency more than any other in the North East! • ATTORNEY OWNED AND OPERATED: Our practices and policies adhere to the standards set forth by the American Society of Reproductive Medicine (ASRM), the Federal Drug Administration (FDA) and the New York Bar Association. • NO WAITING: Immediate consideration by couples intending to cycle now • MANAGABLE TIME COMMITMENT: Our staff is committed to donor advocacy and we strive to minimize the time and inconvenience required. We work closely with you to manage appointments to meet both your scheduling needs as well as clinic requirements • GUARANTEED PAYMENT: At the time of egg retrieval, you will be entitled to receive between $5,000 and $10,000 per donation REQUIREMENTS: • Education: Matriculating or completed with College • Age: 21-30 • Non-Smoker (you will be tested for nicotine) • Healthy Lifestyle (you will be tested for infectious diseases) • Healthy height/weight proportion (BMI < 30) • Healthy past medical history • Good family medical history ]]>

<![CDATA[Position supporting Laboratory Research environment. Our client in greater Boston area is looking for a level 2 / level consultant w/GLP {good lab practices} and some exposure to wet chemistry. Duties vary: -Coordinating validation or instrumentation, server support. -Experience troubleshooting communications issues and network laboratory equipment. -Consultant must have lab and or bio tech experience as well as be able to interface directly w/scientists. Other Responsibilities: -Implement laboratory computer projects including new system deployment and auditing. -Audit adherence to in-house Quality System SOPs, and demonstrate compliance with FDA requirements of 21CFR part 11. -Supply support and training for preclinical and clinical application programs and instruments. -Execute application and operating system software installations/upgrades for all lab computers. -Knowledge of Networked Windows NT/2000 laboratory computers for use of shared file and printing resources. -Deploy all new HPLC/GC instruments, hardware and software. -Maintain and documented changes to laboratory computer resources. Duration: 6 months + extension is likely Rate: $30-$40 hour DOE Location: Cambridge MA If you have interest in this position, please contact me immediately. GTT has over 8 years of experience in IT consulting, including staff augmentation and project engagements. We offer health insurance, 401K, and disability insurance to W2 employees. Also, we will contract on a Corp to Corp basis. Please send Word version of resume to biotechjobs@grouptechinc.com and reference this ad when applying. ]]>

<![CDATA[Provide overall Medical project management to large mega-trials, Call-Center Trials, Pharmacovigilance (PhV) projects, Independent Data Safety Monitoring Boards (IDSMB), and Clinical Endpoint Committees (CEC). General areas of responsibility for Medical Project Management include: ensuring that serious adverse event (SAE) reporting procedures are generated prior to project start; global tracking of serious adverse events; ensuring team compliance with the SAE procedures; regular communication with team members and project management; ensuring appropriate resources are available for the project; overall management of safety activities; ensuring that timelines and client deliverables are met, and financial tracking for Medical. Education: B.S./B.Sc./B.A. in a science or industry-related discipline. Minimum Work Requirements: 5 or more years of relevant work experience recommended. ]]>

<![CDATA[New England Testing Laboratory is looking for full-time laboratory technicians and customer service representatives. Candidates with a science degree or background are encouraged to apply as are recent college graduates. Please send resume and cover letter to work@newenglandtesting.com.]]>

<![CDATA[Job Summary: The Clinical Trials Specialist II role is to efficiently and expertly perform start up activities inclusive of site regulatory document collection, Clinical Study Agreement negotiations, and clinical document review services (review clinical investigator site regulatory package documents, and protocols as related to informed consent forms). The Clinical Trials Specialist II also participates in assigned Clinical Operations initiatives aimed at improving internal standards and systems. This person will also be a mentor to Specialist I and Associate level staff. Position can be located in the Durham, NC, or Waltham MA office Key Accountabilities • Negotiate contracts between sponsor and sites. • Collect and review site regulatory documents. • Assure that project tracking and CTMS is up to date and accurate to meet the project related timelines and contractual obligations. • Participate in the ongoing identification and maintenance of project-specific “Fallback Language” log. • Review and approve investigator site regulatory package documents (Statement of Investigator, CVs, IRB/IEC approval documentation, informed consent form documents, etc.). Work with the appropriate project team members to resolve issues and queries related to SRPs. • Maintain a working knowledge of, and assure compliance with, applicable ICH Guidelines, Good Clinical Practices, Regulatory Agency requirements, and PAREXEL WSOPs. • Participate in Clinical Operations meetings and training initiatives, project team meetings, and maintain relationships with other departments, clients, and regulatory agencies as necessary. • Participate in PXL and department system/standards improvement activities. • Support efforts for generating business leads (client networking, public speaking, etc.). • Provide weekly trackers and accurate monthly metrics in a timely manner to Clinical Operations management. Skills • Demonstrated ability to successfully manage a full workload across multiple-projects. • Above average interpersonal skills. • Ability to understand and maintain client confidentiality • Interpersonal skills and ability to manage multiple projects required • Extensive use of telephone and face-to-face communications which requires the accurate perception of speech • Comprehensive knowledge of relevant software: Windows, Word, Excel, Outlook. • Excellent negotiation skills • Organized with solid oral and written communication skills • Solid analytical and problem-solving skills Education • 4-year degree or relevant clinical or business equivalent. Language Skills • English Minimum Work Experience • Minimum of 2-3 years work experience, one of which has been involved in contract negotiation, site regulatory document collection and review, and/or clinical site monitoring. **Interested candidates should send the CV/Resume in a MS Word document to lindsay.eraso@parexel.com.** For over 25 years PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, we supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. We have helped over 800 clients to develop and launch some of the most important drugs and devices of our time—helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world. For more information about PAREXEL International visit www.PAREXEL.com. ]]>

<![CDATA[Profile: * Understand and maintains the database schemas. * Maintains the system, and data dictionaries * Develops and manages the system meta-data * Maintains the coding processes, standards and templates * Performs source system analysis (what data lives in - what system - what database - what schema - what table - what column - why and how is it used) * Creates and manages source and target data profiles * Gathers, documents and maintains data quality requirements * Gathers, documents and maintains reporting and analysis requirements * Executes, monitors and measures data quality * Gathers, documents and maintains requirements for Business and Data rules for the DW * Reverse engineers existing BO reports to generate existing data quality and reporting requirements * Maps data quality and reporting requirements to physical database schemas. * Manages design documentation Technical Skills * Oracle 9i, 10g RDBMS database development - Senior Level (7+ years) * ERWin Data Modeler - Senior Level (7+ years) * SQL, PL/SQL development - Senior Level (7+ years) * Data Warehousing concepts and practices - Senior Level (7+ years) * Business Objects - Senior Level (7+ years) * Data Modeling - Senior Level (7+ years) * OPA Platform - Senior Level (7+ years) Location: Cambridge, MA Duration: 6 months Rate Target: DOE If you have interest in this position, please contact me immediately. GTT has over 8 years of experience in IT consulting, including staff augmentation and project engagements. We offer health insurance, 401K, and disability insurance to W2 employees. Also, we will contract on a Corp to Corp basis. Please send Word version of resume to biotechjobs@grouptechinc.com and reference this ad when applying.]]>

<![CDATA[Engineering Manager - Facilities Ops Job Description: Our client, a leading bio/pharma company, has an immediate opening for a Facilities Engineering Manager in their Milford location. Qualified candidates will be responsible for managing the engineering functions associated with daily manufacturing operations. Major requirements will include equipment maintenance and calibration, specification and procurement of capital equipment, as well as supervision and motivation of team members. Job Responsibilities: -Manages the maintenance of all facility utilities to ensure proper calibration and operation -Responsible for the maintenance of process equipment, including anticipating problems, assisting in troubleshooting and ensuring equipment availability. -Oversee the planned maintenance program for all equipment, while maintaining exceptional records and monitoring of all modifications and improvements -Manages the execution of capital projects, including space planning and compatibility with existing equipment and processes -Manages and executes an effective calibration programs and is responsible for all equipment operating within specifications and safety parameters. Job Qualifications: -BS/MS in Process or Chemical Engineering -Previous Management training -10 years experience in a Pharmaceutical Engineering/Maintenance roles -Strong written and oral skills are a must -Previous demonstration of leadership -Experience in a GMP environment where precise record keeping is critical -Experience working in a FDA-regulated environment -Experience working in a clean room If you feel qualified for this position, please contact Angela Manley at 781-356-6917 or email resumes to AManley@aerotek.com for immediate consideration. Required Skills: CLEAN ROOM FACILITIES ENGINEER GMP About Aerotek: Join Aerotek CESM, one of the leading providers of engineering and engineering support professionals in North America. Due to our growth, we're constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across a number of different industries. We know it's more than just your day-to-day responsibilities that can make or break a job. It's the support you get. That's the reason Aerotek CE offers a variety of benefits including medical, dental, optical, 401k, and many more. Don't put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek CE team! Allegis Group and its subsidiaries are equal opportunity employers. ]]>

<![CDATA[I’m a recruiter with Discovery Solutions and I’m currently working with a company in the Boston area to fill the position of Manufacturing Data Analyst/Deviation Investigator. I’ve attached the job description and requirements below. If you believe you are a good fit for this position please email me a copy of your resume for consideration and include the job title in the subject one your email. This position does require industry experience…. If you do not have any industry experience please do not apply. Job Description Summary: This company is one of the world's leading suppliers to the pharmaceutical, healthcare and life -science industries. With over 40 locations around the world, it offers products and services that span the product development process -- from research through final product manufacture. The global leader in the production and support of active pharmaceutical ingredients both chemically as well as biotechnologically. We have opening for Manufacturing Data Analyst/Deviation Investigator. In this new position, you will work with organization leadership and staff to assess training needs and recommend appropriate actions to ensure that company location is compliant with required regulatory standards. Lead investigations working with Quality, MTS, R&D, and Manufacturing on critical and major manufacturing deviations to determine root cause, assess product impact, and recommend effective corrective actions. Establish data spreadsheets capturing all critical information for each manufacturing process Monitor data for process trends and shifts. Notifies appropriate personnel when observed (MTS, Quality, Product Management, Manufacturing, etc.) Collaborate with internal groups to determine and implement appropriate measures to prevent the manufacturing process from reaching an out of specification/out of trend state Prepare and presents routine data summary reports for each manufacturing process Provide input to Technical Writers for campaign summary reports Monitor departmental metrics and reports progress against goals Collaborate with internal groups to determine and implement preventative measures to reduce/eliminate repetitive deviations Required Experience Biotech or pharmaceutical manufacturing industry experience. Deviation investigation, Data trending,/analysis Good written and oral skills are essential. Ability to sit for extended periods of time Ability to type for extended periods of time Ability to stand for short periods of time Ability to work in clean room manufacturing environment Must be capable of working independently with minimal supervision Excellent interpersonal skills Highly organized; strong attention to detail; able to effectively interface with people. Must be able to use Word, Excel, JMP and/or other statistical software. Experience with Trackwise a plus. Ability to analyze/interpret manufacturing data. Have strong working knowledge of cGMP and keen problem solving and investigation skills. ]]>

<![CDATA[About the Job This position offers the qualified candidate the responsibility for maintaining, and implementing validation protocols for our new Fall River, MA Cell Culture Facility. This person will oversee and review current validation processes and procedures to ensure compliance with regulatory agency validation requirements as well as industry standards. The Validation Associate will assess and make recommendations for change and improvements in Compliance by working closely with the Quality Assurance Department at Celldex. Other responsibilities include supporting validation efforts for Phase I clinical GMP manufacturing and GLP research at our Needham, MA facility as well as assisting with our Metrology program. Also there will be responsibilities assisting the Facilities department as needed with general facility related issues. The qualified candidiate will have a Bachelors degree in life sciences and 3-4 years validation experience. Biotech/Pharma industry experience desirable. Required skills include excellent verbal and written communications skills, detail oriented, and willingness to be a team-player. Some travel to Celldex sites may be required. To learn more please visit <a href="http://www.celldextherapeutics.com/" rel="nofollow">http://www.celldextherapeutics.com/</a> ]]>

<![CDATA[Description of Position: This position is part of the Research Informatics Application Support Team and is specifically focused on those software applications associated with the company’s small molecule platform. The position will encompass the following responsibilities: • Analyzing and troubleshooting problems encountered by Medicinal Chemists or Computational Biologists related to vendor and custom software applications • Managing license and maintenance contracts for assigned applications • Performing application installations and upgrades • Testing applications prior to equipment and version upgrades • Following required procedures to coordinate with IT on all installations, upgrades and purchases • Participating in the creation of system and support documentation for custom applications • Maintaining all required documentation and records A familiarity with the following software applications or technology areas is preferred. • CambridgeSoft ChemOffice Suite, Various MDL Databases, ChemSW CisPro, Accelrys Accord Enterprise and Excel for Accord, Chemistry eNotebooks, in vitro assay data management. Job Requirements: • 2 years as a systems administrator of applications in a Windows and/or Unix environment • 3 years supporting users and applications in an environment with a mix of Windows, Unix, and Mac • Operating systems • 3 years experience as a chemist in a medicinal chemistry, process chemistry or related role. • Excellent communications and customer service skills • Proven problem solving/troubleshooting skills • Preference for collaborative, team environment • Working knowledge of version control tools Education: • BS in Chemistry and BS or equivalent certifications in Computer Science Location: Cambridge, MA Duration: Long term with 90 day evaluation period Rate Target: DOE If you have interest in this position, please contact me immediately. GTT has over 8 years of experience in IT consulting, including staff augmentation and project engagements. We offer health insurance, 401K, and disability insurance to W2 employees. Also, we will contract on a Corp to Corp basis. Please send Word version of resume to biotechjobs@grouptechinc.com and reference this ad when applying.]]>

<![CDATA[ Fisheries Specialist II Job Location: Work Schedule: Monday-Friday Travel Required: Yes, up to 30% Salary: Commensurate with experience, plus benefits Contact Person: LeShan Witherspoon (lwitherspoon@remsainc.com) Date Available: Immediately REMSA Inc. (www.remsainc.com) is seeking an experienced, highly motivated, and results oriented Fisheries Specialist opening in the Jamestown, RI area. The incumbent must be familiar with the process for properly obtaining, recording, and handling fishery samples of commercially important species as set forth by NMFS as well as the fishing industry in the Northeastern U.S. JOB DESCRIPTION: The incumbent will be charged with collecting and processing samples of various commercially important fish species, with processing data obtained from vessel trip logs, and communicating directly with fishermen and dealers throughout Rhode Island in order to ensure compliance with State and Federal permit requirements and the continued success of the agency’s program. The incumbent will work side by side with State and Federal personnel to ensure that the project continues to provide valuable information on the state of both the fishing industry & important species in Rhode Island. You will be the liaison between the agency and the awardees working to resolve issues and monitor progress towards the program’s goals. Duties include, but are not limited to: • Build and maintain good rapport with those within the commercial fishing industry and state and federal regulatory agencies • Performing port visits to gain obtain biological samples from dealers and fishing vessel as they come into port in order to adequately record valuable information on commercially important species of finfish and shellfish • Process age samples for storage and record data on all samples held • Log and maintain data collected by fishermen and reported in trip logs that are then submitted per permit requirements • Maintain current information in files for samples • Generate performance and compliance reviews and reports for Narragansett Bay Cooperative Study • Serve as the primary Point of Contact for the agency communicating with permit holders to answer questions in regards to requirements for maintaining and renewing commercial fishing permits REQUIREMENTS: Valid Driver’s License and clean driving record is required Ability to pass a background investigation & to obtain security clearance required Education: B.S. in Fisheries Science, Aquaculture, or relevant field is preferred. 2-3 years of field experience. Skills: A background in commercial fisheries, biological sampling and field work, and state and federal research in fisheries industry. • An understanding of the fishing industry in the Northeastern U.S. and the issues and pressures it is subject to • Knowledge of and experience with the sampling protocols set forth by NMFS • Strong biological laboratory skills, including sample processing and storage • Strong data entry skills • Strong interpersonal skills and communication skills, both written and verbal. A professional demeanor • Strong analytical skills, excellent attention to detail, and the ability to understand complex technical information • Excellent time management skills and the ability to work under deadlines and balance multiple assignments • The ability to travel as necessary • Strong computer skills including knowledge of MS Word, Excel, and Access to generate reports and documents • QA/QC experience is helpful BENEFITS: This is a Full Time position, with salary based on qualifications and experience Benefits package includes: 401k, Life Insurance, Short & Long Term Disability, Leave Accrual, etc. For immediate consideration, please email current resumes and cover letter to recruit@remsainc.com or FAX to 757.722.4571 Please refer to position title in responses. Be sure to include all paid and unpaid work experience. Application deadline is Monday November 3rd, 2008 ]]>

<![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[We are a young life sciences (biotech) company looking to hire an engineer/physicist/biophysicist. This is an opportunity to do great science in an exciting for-profit environment. Requirements: -A bachelor's degree or higher in a hard science (engineering/ physics/ biophysics/ physical chemistry/ etc) -A sharp intellect -The desire to work hard and contribute to a company's success and hopefully improve medicine -The ability to start immediately Please respond with salary requirements (important!) and a resume. ]]>

<![CDATA[Position Summary: Will be responsible for performing general laboratory tasks of a very simple and / or repetitive nature. Will work under the direct supervision of a Scientist, Group Leader, Assistant Manager or Manager. Essential Job Duties and Responsibilities: • Performs routine laboratory services such as cleaning glassware, media preparation and sterilization, ordering of cleaning supplies, recording daily temperature on sample refrigerators and freezers, or simple routine calibrations of equipment. • Prepares samples for analysts to perform tests. • Helps in maintaining an organized lab area. • Other duties and job related activities as assigned. Job Requirements: Education: Biotech Certificate, Associate or Bachelor degree in a life science, food science or related discipline. Experience: Previous experience in a laboratory environment preferred. Email resume as attachment to: jobs@cwsciences.com Candidates must live local and be a US Citizen or Permenent Resident Green Card Holder Commonwealth Sciences, Inc. <a href="http://www.cwsciences.com" rel="nofollow">http://www.cwsciences.com</a> ]]>

<![CDATA[Do you like challenges? If so – you will love this job! Autocrat has an immediate opportunity for an entry level quality control technician to support our expanding growth in our extract manufacturing plant. You will be performing a wide variety of lab duties, including, conducting routine daily, weekly, and monthly testing to assure the quality of all raw materials, in-process and finished goods. We are looking for a highly motivated self starter with a Bachelors Degree in Food Science, Technology or similar Math/Science field. You must have excellent communication skills, both verbal and written. Ability to taste differences in products; good sense of smell and taste, and a good judgment of color variations are necessary traits for this position. Autocrat is a company on the move. We are looking for a strong team player who is a self starter and can work on projects from start to finish with little supervision. The successful candidate will support our quality initiatives and help us continue to grow. We need someone who is energetic and enthusiastic who will be able to support our customers. If this sounds like you, please send us your resume!]]>

<![CDATA[We are a 7-person life sciences company looking to fill an entry-level scientist position. Requirements: An undergraduate degree or higher in biology, biochemistry, engineering, physics, or related discipline A desire to work on exciting research with a real possibility to improve medicine/human health The ability to work hard and "get things to work" Please respond with a resume and salary requirements.]]>

<![CDATA[Association of Public Health Laboratories (APHL) is offering an Environmental Public Health Fellowship opportunity, to be hosted at the Rhode Island State Health Laboratory in Providence, RI. The goal of the fellowship is to provide specialized training for a qualified post-graduate level fellow and for the fellow to participate in a research project involving clinical testing for environmental exposures (biomonitoring). The fellowship duration will be one year, with the possibility of extension to a second year, subject to approval by APHL. Interested candidates should possess the following qualifications: · Ph.D. or MS in Chemistry, Biochemistry or Environmental Health with an A average in the chemistry courses. · Interest in environmental health research · Experience with mass spectrometry and chromatography, especially HPLC · Experience with analysis of trace chemical contaminants in clinical specimens · US citizenship is required To apply, please submit a resume and a letter of interest to: Ewa King, Ph.D., State Health Laboratory, Rhode Island Department of Health, 50 Orms Street, Providence, RI 02904. ]]>