Offer summary
Qualifications:
Bachelor's Degree in Life Sciences or similar, Familiarity with PC-based computers and standard software, Knowledge of drug development/clinical trials process, Experience in a pharmaceutical environment preferred, Knowledge of 'good clinical practices' preferred.
Key responsabilities:
- Oversee site activities for study deliverables
- Review and manage study data and quality control
- Manage communications with clinical sites and sponsors
- Assist Project Managers with project administration
- Respond to client inquiries and maintain satisfaction