Offer summary
Qualifications:
Bachelors degree or related experience, 8+ years for Senior role, 10+ for Principal, Proficient in Microsoft Office suite, Experience with clinical database management systems, Knowledge of drug/device development.Key responsabilities:
- Lead data management for clinical projects
- Oversee data entry and quality control processes
- Develop CRF specifications from protocols
- Train personnel on project-specific guidelines
- Communicate with sponsors and vendors on data issues