Clinical Operations Director
4 weeks ago
About the Role
Parexel is seeking a Clinical Operations Leader to join our team in the UK. As a Local Study Associate Director, you will be responsible for delivering clinical studies according to agreed resources, budget, and timelines, complying with Client Procedural Documents, international guidelines, and relevant local regulations.
Key Responsibilities
- Ensure timely preparation of country financial Study Management Agreement (fSMA) and maintain accurate study budget in client clinical studies financial system.
- Lead and optimize the performance of the Local Study Team(s) at country level, ensuring compliance with client Procedural Documents, ICH-GCP, and local regulations.
- Ensure timely submission of application/documents to EC/IRB at start-up and for the duration of the study.
Requirements
- Minimum of 3 years' experience running local clinical trials.
- Proven ability to lead and motivate cross-functional teams to deliver clinical trials according to or ahead of time plan, budget, and with required quality.
- Experience in, and willingness to monitor oncology clinical trials, if needed based on flexible capacity.
About Parexel
Parexel supports clinical studies across the full range of therapeutic areas and has longstanding partnerships with a vast client base. We have a world of opportunity waiting for you, whether you see your future path in fields such as clinical operations, project management, line management, or other positions.
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