Offer summary
Qualifications:
Broad understanding of the pharmaceutical industry, In-depth knowledge of study management and regulatory guidelines, Ability to establish relationships in dynamic environments, Exceptional communication skills for decision-making, Advanced degree or equivalent experience preferred.
Key responsabilities:
- Design and execute clinical studies and trials
- Lead project delivery from protocol to final report
- Manage vendor selection, engagement, and strategy
- Ensure compliance with applicable guidelines and regulations
- Drive change initiatives and propose risk mitigation strategies