When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Parexel is currently seeking a UK Clinical Trial Manager (CTM) to join us at short notice (to start in March 2026), dedicated to a single sponsor.
The Clinical Trial Manager s is responsible for the execution of study-level activities including but not limited to creating and updating trial-specific documents, vendor oversight & delivery, compound training and country and regional oversight of CRO operational delivery.
This includes alignment on the feasibility strategy, target setting, risk reviews, and country challenges that could impact overall study delivery.
Expect exciting professional challenges in inspiring studies, but with time for your outside life.
Responsibilities
Manage integration of project team activities
Manage strategic study operations including but not limited to study sites and tracking systems for regulatory submissions, drug supply and use, enrollment of subjects, regulatory document flow, study timelines, budget and financial information, performance metrics, and data flow
Provide input on trial level operational strategies for clinical trials from protocol design to the final clinical study report for specific studies
Provide input into global subject/patient recruitment plans
Manage aspects of CRO/vendor identification and the day-to-day operational management activities of CROs and other vendors including set up, statement of work creation, and budget oversight
Here are a few requirements specific to this advertised role.
Bachelor’s, nursing degree or equivalent required, science preferred.
Minimum 5+ years of clinical research experience gained with a CRO, biotech or pharmaceutical company working on phase I-IV global clinical trials
2-3 years leading aspects of clinical trials
CRO oversight experience is essential
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