Offer summary
Qualifications:
Associates degree preferred or equivalent, Experience in clinical research/pharma/biotech, Good knowledge of medical terminology, Familiarity with ICH/GCP standards, Strong organizational skills.
Key responsabilities:
- Perform site management activities and ensure protocol compliance.
- Maintain project files, manage documentation and communication.
- Assist in team meetings and coordinate resources.
- Track clinical and regulatory documents for researcher sites.
- Train junior Clinical Operations Specialists as needed.