Offer summary
Qualifications:
Bachelors degree or related experience, 8+ years for Sr. CDM, 10+ for Principal CDM, Proficiency in Microsoft Office, Familiarity with clinical database systems, Experience in drug/device development.
Key responsabilities:
- Manage clinical trial data process from startup to post-lock
- Oversee data entry processes and quality control
- Develop CRF specifications and maintain documentation
- Coordinate with third-party vendors for timelines
- Lead training sessions for study personnel