At a Glance
- Tasks: Manage study activities and ensure timely tasks in infectious disease trials.
- Company: Join Medpace, a leading international CRO with a focus on clinical trial management.
- Benefits: Gain valuable experience, receive training, and access career advancement opportunities.
- Other info: Dynamic team environment with a clear path to leadership roles.
- Why this job: Kickstart your career in clinical project management and make a difference in healthcare.
- Qualifications: PhD graduates with a passion for clinical research and project management.
The predicted salary is between 25000 - 32000 £ per year.
Medpace is seeking a full-time, office-based Associate Clinical Trial Manager (a CTM) to join our Clinical Trial Management team.
The role offers an entry path for Ph D graduates into clinical project management within an international CRO setting.
You will work with Project Coordinators and Clinical Trial Managers to manage study activities, ensure timely tasks, and maintain project documentation.
Training will be provided and the career path leads toward CTM leadership.
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PhD Associate CTM: Infectious Disease Trials 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.
