Daily Rate:
£500/day PAYE/ Umbrella
Essential Requirements:
- University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.
- Relevant experience from within the pharmaceutical industry or similar organization or academic experience
- Knowledge of clinical development/ drug development process in various phases of development and therapy areas
- Excellent knowledge of international guidelines ICH/GCP
- Good project management skills
Global Study Manager Role:
- Provides oversight to ensure study delivery & leads/contributes to the preparation of delegated study documents (e.g., Informed Consent Form, master Clinical Study Agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions, presentations etc.).
- Maintains and facilitates interactions with internal functions and external functions including the CROs to ensure an efficient study delivery to time, costs and quality objectives.
- Contributes to the planning and conduct of internal and external meetings (e.g., Investigators’/Monitors’ meeting).
- Proactively contributes to risk and issue identification, development of mitigation and/or action plans for identified risks and issues.
Company:
Our client is a global research-based bio pharmaceutical company with a major UK presence who are committed to making a meaningful impact on people’s lives with life-changing medicines. This is a worldwide brand name which will not only look fantastic on your CV for years to come but also offer inspiring and rewarding work.
Location:
This Global Study Manager role is fully remote.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 56471 in all correspondence.