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
- Provide input to the study budget and is responsible for managing assigned vendor budgets
- Provide drug supply assumptions to clinical planning team
- Conduct protocol and site feasibility assessments
Requirements:
- 5+ years direct industry study management experience in clinical and drug development
- Bachelors degree or equivalent undergraduate degree
- Working knowledge of international regulatory and ICH GCP guidelines
- Experienced in clinical trial management
- Experience in planning, risk mitigation strategies, trial budgets, site selection, clinical supplies management, conduct and monitoring of clinical studies
- High level of initiative and ability to work independently
To find out more about Real please visit www.realstaffing.com