Senior Study Physician — Clinical Trials Lead

Parexel; United Kingdom; On-site; GBP 80,000 - 110,000; Full time

Job summary

Parexel is seeking an experienced Study Physician to join in the UK or Germany. You will be medically responsible across the clinical trial lifecycle, providing medical oversight from design to final report.

The role is dedicated to a single client, ensuring high-quality protocols, contributing to risk-based quality management, and co-authoring monitoring plans. Prior pharma/CRO medical monitoring experience is highly valued.

Qualifications

• MD (Physician) with clinical training and minimum 4 years of active clinical practice.
• Specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology or Emergency Medicine is highly desirable.
• Experience in pharma industry or CRO in medical/project management or pharmacovigilance is desirable.

Responsibilities

• Medically responsible at the trial level throughout preparation, conduct and reporting.
• Provide medical expertise and oversight from Trial Design Outline to Clinical Trial Report.
• Dedicated to one client and ensure high-quality trial protocols with minimal amendments.
• Contribute to risk-based quality management by defining data and risks in the plan.
• Co-author Clinical Quality Monitoring plans and perform ongoing reviews of medical data.

Skills

Clinical trial oversight

Medical monitoring

ICH-GCP knowledge

Regulatory compliance

Education

MD (Physician)

Tools

CTMS

EDC systems

Job description

Parexel is seeking an experienced Study Physician to join in the UK or Germany. You will be medically responsible across the clinical trial lifecycle, providing medical oversight from design to final report.

The role is dedicated to a single client, ensuring high-quality protocols, contributing to risk-based quality management, and co-authoring monitoring plans. Prior pharma/CRO medical monitoring experience is highly valued.