Job Summary
A clinical research organization needs applicants for an opening for a Remote Clinical Research Associate.
Core Responsibilities Include:
- Conducting monitoring to confirm subject safety and data integrity
- Monitor the progress of clinical studies at investigative sites or remotely
- Assisting team lead in the development of trial tools or documents
Must meet the following requirements for consideration:
- Monitor the progress of clinical studies at investigative sites or remotely
- 2+ years of clinical monitoring experience and clinical research experience
- Knowledge of ICH and local regulatory authority regulations regarding drug
- Read, write and speak fluent English; fluent in host country language
- An advanced degree (e.g., M.S., M.B.A., PharmD, etc), Licensed health-care professional (i.e., registered nurse)
- Experience in monitoring all trial components (PSSV to COV) and experience in coaching/mentoring other CRAs