Clinical Research Coordinator
Trenton Metro Area, NJ
- BS in nursing or related with at least 5 years as a clinical research coordinator
- Strong background in GCP, CTMS, Adverse Events Reporting
- Oversight of research protocol to the clinical setting .
- Maintains appropriate documentation associated with the assigned clinical study.
- Ensures studies are conducted according to established company policies and procedures as well as all Good Clinical Practice (GCP), ICH, and FDA guidelines.
- Obtains informed consent according to GCP
- Schedules subject visits
- Prepares labs/tests per protocol
- Completes case report forms (CRFs) in timely manner