Offer summary
Qualifications:
5+ years minimum experience in data management, Bachelor's degree or related experience, Proficiency in Microsoft Office Suite, 1+ years of leadership experience, Broad knowledge of drug and device development.
Key responsabilities:
- Manage daily activities of Clinical Data Associates
- Oversee clinical trial data management processes
- Coordinate inter-departmental communication
- Develop and maintain Standard Operating Procedures
- Provide input on project timelines and resource needs