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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
Job Description
Company Description


Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labeling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.


In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.


Eurofins BioPharma Product Testing has delivered expert scientific support to companies working to improve human and animal health. As a member of the Eurofins BPT team, you will work alongside respected technical experts dedicated to scientific excellence in a process driven regulatory compliant environment.



Supervise and assist in the conduct of regulatory studies performed. Responsibilities include:


  • Responsibilities as stated in GLP regulations.
  • Client liaison.
  • Data interpretation and report writing.
  • Assist in protocol development, design and implementation.
  • Supervise study conduct.


Management Responsibilities


  • 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.


Technical Responsibilities


Overall responsibility for the technical conduct of all studies and interpretation, analysis, documentation and reporting of results. Specifically:


  • 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.


Any other duties assigned.


Qualifications


  • 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.


Additional Information


Position is full-time, Monday-Friday, 9:00am.- 5:00 pm, with overtime as needed. Candidates currently living within a commutable distance of Dayton, NJ are encouraged to apply.


#LIPO1


Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.