Description
Job Responsibilities:- Provide leadership and support to one or more global study teams within an early development program
- Responsible for vendor selection and management including CRO, IVRS, central lab and imaging vendor
- Conduct protocol and site feasibility assessments
- Provide input to the program budget and is accountable for managing overall study budget
- Accountable for Clinical Operations deliverables to achieve study objectives and milestones within timelines and budgets
Requirements:
- 5+ years direct industry study management experience in clinical and drug development
- Bachelors degree or equivalent undergraduate degree in a scientific discipline
- Working knowledge of international regulatory and ICH GCP guidelines
- Familiar with global trial requirements
- Experienced in clinical trial management
- Strong analytical skills
To find out more about Real please visit www.realstaffing.com