Study Physician - Remote - UK - Register your interest

Parexel; Uxbridge; Remote; GBP 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a dedicated Study Physician to play a pivotal role in clinical trials. This exciting opportunity involves overseeing the medical aspects of trials from design to reporting, ensuring high-quality protocols and risk management. The ideal candidate will have a strong clinical background, ideally with specialization in internal medicine or general practice, and experience in the pharmaceutical industry. Join a forward-thinking company that values medical expertise and contributes to groundbreaking clinical research.

Qualifications

• Minimum 4 years of active clinical practice as a physician.
• Experience in the pharma industry or CRO is desirable.

Responsibilities

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

Skills

Clinical Practice

Medical Oversight

Pharmacovigilance

Data Visualization

Project Management

Education

Physician (MD)

Medical Thesis

Tools

Clinical Trial Management Systems

Data Analysis Software

Job description

Parexel is currently seeking an experienced Study Physician to join us in the UK. This role involves being 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 clinical trials. You will provide medical expertise and oversight from the Trial Design Outline to the Clinical Trial Report, playing a core role within the trial team.

Key Responsibilities

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

Requirements

• Physician (MD), ideally with a medical thesis, trained in a clinical setting, with a minimum of 4 years of active clinical practice. Specialization in internal medicine or general practice is desirable.
• Experience in the pharma industry or CRO in medical, project management, or pharmacovigilance functions, preferably in Clinical Development.
• Understanding of relevant regulations and guidance, including ICH-GCP.
• Experience with data visualization and IT systems is a plus.
• Clinical development/trials experience is an additional asset.

Additional Information

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Healthcare Provider
• Industry: Pharmaceutical Manufacturing