Job Summary
A company dedicated to the future of clinical developmentpivotal or supportive trials that led to FDA and/or international regulatory approval of 50+ such drugs is in need of a Telecommuting Entry Level Clinical Research Associate.
Core Responsibilities of this position include:
- Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH-GCP guidelines
- Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sites
- Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely
Position Requirements Include:
- 3 years of Study Coordinator experience required
- Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required
- Clinical research experience
- Knowledge of ICH and local regulatory authority regulations regarding drug
- An advanced degree (e.g., M.S., M.B.A., PharmD, etc)