Description
Roles and Responsibilities:- Develops operational plans including site monitoring strategies, risk mitigation strategies, trial budgets, site selection, and clinical supplies management
- Develops and maintains effective working relationships with SMT members, with particular focus on affiliate teams, external CRO and co-development partner study teams
- Contributes to the development and management of the study timelines, resources, budgets, risk and quality plans
- Establishes study milestones and ensures accurate tracking and reporting of study metrics
Requirements:
- Life sciences degree or nursing equivalent or substantial experience in a clinical research/healthcare enviornment
- Good knowledge of ICH GCP guiedlines
- Experience working as part of a large team and leading small study or functional teams, with a proven ability to be an active member of the team and motivate and lead a small team to deliver against commitments
- ***Immunology type background with experience in the gastrointestinal disease area (preferred)
To find out more about Real please visit www.realstaffing.com