Offer summary
Qualifications:
Bachelors or related experience required, 8+ years experience for Sr. role, 10+ years experience for Principal role, Proficiency in Microsoft Office Suite, Experience with clinical database management systems.
Key responsabilities:
- Manage all aspects of clinical trial data process
- Oversee project data entry and quality control
- Develop CRF specifications and maintain documentation
- Liaise with third-party vendors for deliverables
- Train clinical research personnel on project items