Job Summary
A clinical research organization is seeking a Telecommute Clinical Research Associate.
Core Responsibilities Include:
- Monitoring the progress of clinical studies at investigative sites or remotely
- Ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol standards
- Conducting monitoring to confirm subject safety and data integrity
Must meet the following requirements for consideration:
- Travel to clinical trial sites
- An advanced degree (e.g., M.S., M.B.A., PharmD, etc)
- Clinical research experience
- Read, write and speak fluent English; fluent in host country language required
- Knowledge of ICH and local regulatory authority regulations regarding drug
- Experience in monitoring all trial components (PSSV to COV) Experience in coaching/mentoring other CRAs
