Clinical Research Coordinator
PALO ALTO, CA, USA. FULL-TIME/PART-TIME
Supporting clinical research staff and managing new and ongoing clinical research activities.
Assisting clinical investigators and research staff to drive projects forward by interacting closely with other teams.
Communicate clinical trial status to management and staff through meetings and tracking system; maintain related records.
Clinical Study Coordinator will adhere to FDA guidelines in the conduct of all study-related activities.
B.S. or B.A. degree required.
Knowledge of good clinical practice, FDA, OHRP, HIPAA policies.
Familiarity with Microsoft Word and Excel.
Excellent organizational skills to independently manage workflow.
B.S. degree in basic sciences, a similar technical field of study or equivalent practical experience.
5+ years of experience as a Clinical Study Coordinator/ Clinical Research Coordinator is preferred.
Certified Clinical Research Coordinator (certification through ACRP or SOCRA)
Job type: Full-time.
U.S. citizens, green card holders, and those authorized to work in the U.S. for any employer will be considered.