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Associate Study Coordinator
•30 days ago
| Hours | Full-time, Part-time |
|---|---|
| Location | Somerset, New Jersey |
About this job
Job Description Job Overview: Individual has responsibility for coordinating the activities of routine and non routine studies for in vivo PK in compliance with appropriate company standards, GLP, GCP, GMP and regulatory guidelines specified in the study plans, protocols, or work agreements governing the work in which they are involved in a timely, efficient and quality manner. * Trains and mentors less experienced staff * Able to review work of others for overall accuracy, timeliness, completen
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