Description
Primary Responsibilities include but not limited to:- Develops site monitoring strategies, risk mitigation strategies, trial budgets, site selection, and clinical supplies management
- Assists in building efficient high performing operations teams and ensures team members are aware of their accountabilities, responsibilities and deliverables
- Contributes to the development and management of the study timelines, resources, budget, risk and quality plans; develops and manages clinical study budgets and contributes to staffing/resourcing plans
- Establishes study milestones and ensures accurate tracking and reporting of study metrics
Skills / Experience:
- Clinical development experience in all operational aspects of clinical studies
- Experience working in a global environment and/or including monitoring or leading affiliate teams, working with vendors and/or CROs, drug supply management and planning operational activities to achieve database lock
- Experience in Phase I - IV trial management including development of timelines, budgets and resource plans
- Experience working as part of a large team and leading small study or functional teams
- Well developed written and verbal communication skills
- Pharmaceutical / Biotech industry experience
To find out more about Real please visit www.realstaffing.com