Offer summary
Qualifications:
Bachelor's Degree in Life Sciences or similar, Familiarity with PC-based computers and standard software, Knowledge of drug development and clinical trials, Experience in pharmaceutical environment preferred, Understanding of good clinical practices preferred.
Key responsabilities:
- Oversee site activities ensuring timely study deliverables.
- Review and monitor study-related data, resolve discrepancies.
- Manage communications with clinical sites and sponsors.
- Assist Project Managers in project administration and timelines.
- Adhere to SOPs and participate in modifications.