Description
Primary Responsibilities:- Independently lead cross-functional Study Teams.
- Responsible for Phase I unit site selection; CRO vendor management and oversight.
- Provide input to the program budget and manage overall study budget.
- Track timelines, milestones, identify critical study activities and provide regular updates to the study teams.
Skills/Education:
- Highly experienced in managing early development phase I clinical studies
- Extensive experience in planning, risk mitigation strategies, trial budgets, site selection, clinical supplies management, sample management, conduct and comitoring of clinical studies
- Demonstrated experience in various therapeutic areas; experience in conducting healthy volunteer ClinPharm Phase 1 dose escalation studies
- Familiar with global trial requirements
- 6-8+ years study management experience including managing and partnering with Early Phase CRO's to deliver a broad range of CRO services.
To find out more about Real please visit www.realstaffing.com