At a Glance
- Tasks: Coordinate clinical trials and manage study materials in a global team.
- Company: Medpace, a leader in clinical trial management.
- Benefits: Solid training, accelerated career path, and collaborative work environment.
- Other info: Great opportunity for growth in a dynamic industry.
- Why this job: Kickstart your career in the exciting field of radiopharmaceuticals.
- Qualifications: PhD in Radiopharmaceuticals/Nuclear Medicine required.
The predicted salary is between 35000 - 45000 £ per year.
Medpace is seeking an Associate Clinical Trial Manager (Ph D) to join our Clinical Trial Management team in the UK.
The role targets Radiopharmaceuticals/Nuclear Medicine Ph Ds and provides solid foundational training in clinical project administration.
As part of a global team you will coordinate with project coordinators and managers, ensure timely, accurate tasks, and manage study materials and timelines.
This is an excellent entry point into industry with an accelerated career path.
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Associate Clinical Trial Manager – Radiopharmaceuticals (PhD) in Stirling employer: Medspace
As a Project Assistant in Clinical Safety & Pharmacovigilance based in Stirling, you will join a dynamic team dedicated to ensuring the highest standards of safety in clinical trials. Our company fosters a collaborative work culture that values employee growth, offering opportunities for professional development and training. With a focus on meaningful contributions and a supportive environment, we provide an excellent platform for those looking to make a real impact in the healthcare sector.
