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Client:
Parexel
Location:
Uxbridge, United Kingdom
Job Category:
Other
EU work permit required:
Yes
Job Reference:
3ed404290f7e
Job Views:
4
Posted:
16.03.2025
Expiry Date:
30.04.2025
Job Description:
When our values align, there's no limit to what we can achieve.
Parexel is currently seeking an experienced Study Physician to join us in the UK, you will be assigned to one of our key sponsors in the EMEA region. This is an upcoming role, not an active position.
Working as a Study Physician, you will be medically responsible at the trial level throughout the preparation, conduct, and reporting phase of clinical trials. During the clinical trial, you will provide medical expertise and oversight from the Trial Design Outline to the Clinical Trial Report. This is a core role within the trial team.
Some specifics about this advertised role:
* Dedicated to one client.
* Ensure timely preparation of high-quality clinical trial protocols, minimizing protocol amendments.
* Contribute to trial risk-based quality management by defining medically relevant data and related risks integrated into the quality and risk management plan.
* Co-author Clinical Quality Monitoring plans.
* Perform ongoing reviews of medical data.
Here are a few requirements specific to this advertised role:
* Physician (MD) (ideally with medical thesis), trained in a clinical setting, and a minimum of 4 years of active clinical practice experience; specialization in internal medicine or general practice is desirable.
* Experience in the pharma industry or CRO in medical or project management or global pharmacovigilance functions/any other relevant medical function ideally in Clinical Development is desirable.
* Understanding of relevant regulations and guidance including ICH-GCP.
* Ideally experienced with data visualization systems and IT systems.
* *Clinical development/trials experience would be an additional asset.
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