1. clinical research associate
job description: A clinical research associate (CRA) is responsible for conducting monitoring visits at investigative sites that are participating in clinical trials for drugs, devices, biologics, vaccines, diagnostics or combination product. The CRA must follow sponsor SOPs and protocols, ICH guidelines, CFR and GCP/GLP. Their work is preformed in various settings, such as pharmaceutical companies, medical research institutes, hospitals, clinics, Phase 1 research facilities and government agencies.
skills or certifications needed: clinical research, GCP, pre-study visits (PSV), case report forms (CRF), site monitoring, study protocols
skills or certifications needed:
- clinical research
- pre-study visits (PSV)
- case report forms (CRF)
- site monitoring