Study Physician - Remote - UK - Register your interest

TN United Kingdom; Uxbridge; Remote; GBP 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a dedicated Study Physician to join their team in the UK. This role is pivotal in overseeing clinical trials, ensuring the highest standards of medical oversight and protocol management. As part of a dynamic team, you'll be responsible for preparing clinical trial protocols and managing risks associated with trial data. This position offers a unique opportunity to contribute to groundbreaking medical research while working closely with a key client in the EMEA region. If you have a passion for clinical excellence and a background in internal medicine, this role could be your next career milestone.

Qualifications

• Minimum of 4 years of active clinical practice experience required.
• Specialization in internal medicine or general practice is desirable.

Responsibilities

• Ensure timely preparation of high-quality clinical trial protocols.
• Contribute to trial risk-based quality management.

Skills

Clinical Trial Management

Medical Expertise

Regulatory Knowledge (ICH-GCP)

Data Visualization Systems

Education

Medical Degree (MD)

Clinical Practice Experience

Tools

Clinical Quality Monitoring Systems

Job description

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Client:

Parexel

Location:

Uxbridge, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

3ed404290f7e

Job Views:

11

Posted:

26.04.2025

Expiry Date:

10.06.2025

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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. Please note, this is an upcoming role and not an active position.

As a Study Physician, you will be medically responsible at the trial level throughout the preparation, conduct, and reporting phases of 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.

Key responsibilities include:

• Dedicated to one client.
• Ensure the 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, and integrating them into the quality and risk management plan.
• Co-author Clinical Quality Monitoring plans.
• Perform ongoing reviews of medical data.

Requirements for this role:

• Physician (MD), ideally with a medical thesis, trained in a clinical setting, with 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, project management, or pharmacovigilance functions, preferably within Clinical Development.
• Understanding of relevant regulations and guidance, including ICH-GCP.
• Experience with data visualization systems and IT systems is preferred.
• Clinical development/trials experience is an additional asset.