At a Glance
- Tasks: Lead clinical trial operations and manage vendor relationships in a dynamic environment.
- Company: Join Medpace, a top CRO for biotech companies, making a real impact.
- Benefits: Remote work flexibility, competitive salary, and equity options.
- Other info: Exciting opportunity for career growth in a supportive team.
- Why this job: Be at the forefront of clinical trials and drive innovation in Oncology.
- Qualifications: Proven leadership experience in clinical trial management and strong communication skills.
The predicted salary is between 55944 - 68376 £ per year.
Medpace is the leading CRO for biotech companies and is seeking a Director of Clinical Trial Management (operational role) to join our Clinical Trial Management Group in Stirling, UK.
This is an executive, hands-on leadership position.
You will oversee day‑to‑day trial operations, be the primary Sponsor contact for study deliverables, manage vendors and sites, and drive cross‑functional collaboration with a focus on Oncology or related areas.
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Associate Director, Clinical Trials - Remote & Equity 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.
