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<![CDATA[TECHNICIAN ASSISTANT - SAMPLE MANAGEMENT OFFICE Columbia Analytical Services (CAS), established in 1986, is an employee-owned, full-service analytical laboratory network, specializing in environmental and pharmaceutical testing. Our vision is simple: to be the best analytical services company in the industry. (<a href="http://www.caslab.com" rel="nofollow">http://www.caslab.com</a>). LOCATION CAS/Jacksonville, Florida is a full service analytical laboratory providing testing for many industrial, government and consulting firms in the southeastern United States. As with other CAS facilities, CAS/Jacksonville serves international clients, having the necessary permits to accept foreign water and soils in the country for analysis. The laboratory’s technical expertise includes the analysis of routine environmental samples, landfill samples, DOD projects and waste stream characterization. They also perform industry specific testing for pulp and paper manufacturers. CAS/Jacksonville offers field sampling and local courier service. They also provide a variety of customized reports, including electronic data deliverables and full CLP-like packages. DUTIES/RESPONSIBILITES Entry level position within a technical area where work is closely supervised and performed in accordance with well defined standards and procedures of an uncomplicated nature. Position involves utilizing a variety of routine operating procedures and practices, including washing glassware, preparing bottles for sample collection, stocking shelves, general clean-up, receiving client samples, general shipping and receiving, computer data entry, client interaction, and assisting scientific staff. REQUIRED EDUCATION, SKILLS, QUALIFICATIONS High School Diploma desired. Able to lift up to 40 lbs., knowledgeable in common computer programs (Microsoft Word, Excel), strong organizational skills BENEFITS CAS offers a competitive compensation and benefits package, including 401(k), ESOP, health and life insurance, domestic partner benefits, and flexible spending account. Equal Opportunity Employer. Women/minorities/disabled/veterans encouraged to apply. ]]>

<![CDATA[Regional CRA for immediate need. As key team members supporting new drug applications, the Regional CRA is accountable for on-site clinical monitoring activities from study start-up through close-out. As specified in the monitoring plans, the RCRA will perform source document verification review of Case Report Forms, oversee drug accountability, as well as manage investigational site to ensure compliance with FDA regulations, ICH/GCP guidelines, and company SOPs. Requirements: Travel These positions are home-based and require over 50% travel Experience: For you to be the successful candidate we are looking for in these roles you must have a proven track record of monitoring clinical trials in a variety of Therapeutic Areas through the CRO or Pharmaceutical industry Education: For consideration, you must hold a Bachelor's degree, preferably in a scientific or nursing discipline Due to the precise requirements of these positions, we will only be contacting candidates that meet all of the listed criteria. If you are qualified and interested in the excellent career opportunities we have for you, please reply to this ad immediately with your CV and availability. ]]>

<![CDATA[Our client in Savannah, GA is looking for an Analyst I. This candidate must have a BA or BS in Chemistry or related field. Please send your resume for further review. ]]>

<![CDATA[Need help with an American history test if you can get me an A or a B I will give you 50 dollars. The test is from United States history 1865 to Present. There's 40 questions all mutilple choice and and a timer of 1 hour and 30 mins. If you serious email me or give me a call at 904-803-5297.]]>

<![CDATA[Our world class client is seeking a candidate who can perform the following duties: Under general supervision, plans and monitors human clinical trials in compliance with internal procedures, ICH Guidelines, Good Clinical Practices (GCP) and applicable Regulations and Guidelines. Coordinates protocol and case report form development and compilation. Insures appropriate clinical trial agreements are signed and materials are distributed. Monitors and secures protocol and regulation compliance at investigational sites. Reviews, retrieves, and reports the trial data as the requirements dictate or as is appropriate. 1. Monitors clinical study per ICH Guidelines and GCPs. (15%) 2. Maintains essential documents and other study-related documents. 20%) 3. Plans and develops simple study protocols/technical reports, CRFs and other study materials. (15%) 4. Assists in study implementation, which may include: investigator recruitment, site management, IRB liaison, Adverse Event management, Periodic Report generation, and/or supplier oversight. (35%) 5. Performs other related duties as assigned by management, including process improvements. (15%) Bachelors degree or equivalent experience. 3 to 6 years of pharmaceutical/medical device clinical research experience or optometric/ophthalmic technician. Working knowledge of regulations and standards applied in clinical area and medical devices. Working knowledge, understanding and application of principles, concepts and practices of clinical investigations/studies. Strong organizational, analytical, oral and written communication skills. Knowledge of the application of requirements to new products and processes. Ability to collect and analyze data. Ability to develop innovative solutions to problems with minimal complexity. Anthony J. Vilone Aerotek Engineering Division 904-527-5623 ]]>

<![CDATA[ Check out <a href="http://www.JobsInBiotech.net" rel="nofollow">http://www.JobsInBiotech.net</a> Free biotech job listings. No fees, free job listings for job seekers. Enter your city or zip and get results from local and national companies with biotech jobs near you. ]]>

<![CDATA[Wetland Permitting Consultant needed part time for a small consulting firm. Must know: - ArcMap / GIS, MS Office Suite, (CAD & QuickBooks would be a plus) - Wetland delineation methodology - Wetland impact assessments Would like a candidate with the following abilities: - Organization skills, detail oriented nature - Project coordination and follow-up - Ability to work for 2 bosses & work independently - Bookkeeping - Office admin such as mailings, filing, mgmt. of office equipment / supplies - Work under deadlines, often in a fast paced environment - Rapid assimilation and retention of new information and software - Ability to be trusted - background checks, personality tests, and reference checks will be performed Work environment has animals which may bother individuals with allergies.]]>

<![CDATA[look for a bio tutor or someone that has a college background in the bio / scientific field , pay is 15.00 an hour. Must be great at writing and must be able to start asap. Please call 9524651182 if interested. ]]>

<![CDATA[Local manufacturing company is seeking several experienced Sewing Machine Operators. This is a contract to permanent opportunity. Job Description: Must have experience operating sewing machine. Operate single needle, double needle and/or Serger machine. Must be able to work in a high paced production environment. Must be flexible to work overtime and weekends as needed. Must be able to pass a sewing test and follow instructions. Shifts: 1st (6am-3pm) Monday-Friday and 3rd (9pm-6am) Sunday-Thursday Pay Rate: $9.25/hr ($10.25 for working overnight shift) Anyone with any Sewing Machine experience can apply! ]]>