Description
Roles and Responsibilities:- Responsible for Clinical Operations deliverables to achieve study objectives and milestones within timelines and budget
- Responsible for vendor selection and management including CRO, IVRS, central lab and imaging vendor
- Partner with CPL to develop and present at project teams and management review bodies
- Conduct protocol and site feasibility assessments
- Provide input to the program budget and is accountable for managing overall study budget
Requirements:
- Bachelor's degree or equivalent undergraduate degree
- 5+ years direct industry study management experience in clinical and drug development
- Working knowledge of international regulatory and ICH GCP guidelines
- Familiar with global trial requirements
- Excellent planning and organizational skills
To find out more about Real please visit www.realstaffing.com