FOCUS OF THE JOB:
Lead and coordinate the study start-up phase in collaboration with the Project Management and Study Teams, ensuring efficient and compliant initiation of standalone studies or programmes through the effective application of project management principles, methodologies, and processes
KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:
- At least 2 years experience working in clinical trials.
- Demonstrable experience in the management or coordination of clinical trials, ideally gained within a Site Management Organisation, Contract Research Organisation, NHS clinical trials environment, pharmaceutical company, or a comparable setting.
- Knowledge of UK regulatory submissions and Trial documentation would be advantageous.
- Able to plan and prioritise own workload, responding efficiently to requests from multiple project managers.
- Excellent time management, organisation and communication skills
- A life sciences degree/ proven experience in an administration role.
