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Study Director Jobs
Company | Eurofins Lancaster Laboratories |
Address | South Brunswick, NJ, United States |
Employment type | FULL_TIME |
Salary | |
Category | Biotechnology Research |
Expires | 2023-07-31 |
Posted at | 10 months ago |
Company Description
- Responsibilities as stated in GLP regulations.
- Client liaison.
- Data interpretation and report writing.
- Assist in protocol development, design and implementation.
- Supervise study conduct.
- Overall, day-to-day laboratory operation including supervision of technical staff assigned to your studies.
- Scheduling and coordinating initiation and conduct of studies.
- Ensure that the study schedule and financial aspects of each study that you are responsible for are accurately tracked on a regular basis.
- Supervise conduct of all phases of the study, including participation in study conduct.
- Ensure all experimental data is properly recorded and that observations of unanticipated responses of the test system are accurately recorded and verified.
- Ability to safely wear a respirator required
- Develop experimental design and supervise implementation of experiments (tests).
- Instruct, train and supervise scientists in all procedures.
- Ensure that GLP regulations are followed.
- Establish test protocols and corresponding SOP's.
- Obtain sponsor approval of protocols and institute any necessary deviations from the test protocol with sponsor approval.
- Maintain liaison with regulatory agencies in conjunction with: test protocols, and past or present studies submitted for regulatory approval, compliance with GLP's and appropriate test guidelines.
- Ensure tests are conducted in accordance with the test protocol and SOP.
- Interpretation, calculation, analysis, documentation and reporting of results.
- Maintain liaison with sponsors, advising them of test results; and assisting with protocol development.
- Intimate working familiarity and/or ability to quickly learn and develop such familiarity with all government regulations dealing with testing particularly EPA, FDA, DOT, OECD, and GLP regulations in addition to ISO standards.
- Hands-on working knowledge of the tests that will be under their responsibility.
- At least a Bachelor of Science degree or equivalent experience in a field related to their area of responsibility (e.g. animal science, chemistry, biology, microbiology).
- Good administrative skills and leadership ability. Must communicate effectively and write well.
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