Medical Director/Study Physician - UK (Remote) - FSP

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 an experienced Study Physician/Medical Director to join us in the UK. You be assigned to a single sponsors in the EMEA region.

Working as a Study Physician/Medical Director you will be medically responsible at the trial level throughout the preparation, conduct and reporting phase of clinical trial. During the clinical trial, you will be responsible to provide medical expertise and medical 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 medical quality clinical trial protocols, minimising protocol amendments.

• Contribute to trial risk-based quality management, by defining medically relevant data and related risks are integrated into the quality and risk management plan.

• Co-author Clinical Quality Monitoring plans.

• Performing 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 minimum of 4 years of active clinical practice experience; specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, and Emergency Medicine is highly desirable.

• Experience in 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 previous experience as a medical monitor

• Ideally experienced with data visualization systems and IT systems.

• Clinical development/trials experience which would be an additional asset

We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You’ll be an influential member of the wider team.

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