About You
Essential criteria
- First degree in a health sciences or related discipline.
- Knowledge of ICH-GCP, R&D Governance, EU Clinical Trials Directive and Medicines for Human Use (Clinical Trials) Regulations.
- Ability to acquire detailed protocol knowledge and communicate protocol requirements to both professionals and patients.
- Knowledge of research ethics and governance frameworks and ability to facilitate research applications.
- More than two years' experience as a Clinical Trials Coordinator, Clinical Project Manager or equivalent clinical research role.
- Experience working independently and as part of multidisciplinary teams, with excellent interpersonal and communication skills.
Desirable criteria
- Additional qualification in clinical trials or clinical research.
- Experience working within the NHS.
- Project management experience.
- Experience supporting research staff.
- Experience contributing to protocol or study documentation development
Further Information
We pride ourselves on being inclusive and welcoming. We embrace diversity and want everyone to feel that they belong and are connected to others in our community. We are committed to working with our staff and unions on these and other issues, to continue to support our people and to develop a diverse and inclusive culture at King's.
We are not able to offer sponsorship for candidates who do not currently possess the right to work in the UK.
Senior Study Coordinator - INTERNAL ONLY London, GB
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Senior Study Coordinator - Internal Only employer: King's College London
At King’s College London, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our commitment to employee growth is evident through comprehensive training opportunities and a supportive environment that encourages professional development. Located in the heart of London, our institution offers unique advantages such as access to world-class resources and a vibrant community dedicated to advancing research and education.
