Medical Director/Study Physician - CD Inflammation - Remote - Sponsor Dedicated

Overview

In this role, you will provide medical oversight and accountability at the trial level across prep, conduct, and reporting. You join a dedicated sponsor-focused team in the EMEA region, guiding protocol quality and medical data review. You help shape trial design, risk management, and monitoring plans to ensure high medical quality. You contribute to seamless collaboration with cross-functional teams to advance therapeutic development and patient impact.

Responsibilities

• Assume medical responsibility at the trial level from preparation through Clinical Trial Report.
• Provide medical expertise and oversight from Trial Design Outline to Clinical Trial Report.
• Be dedicated to one client.
• Ensure timely preparation of high-quality clinical trial protocols and minimise protocol amendments.
• Contribute to trial risk-based quality management by defining data and associated risks for the quality/risk plan.
• Co-author Clinical Quality Monitoring plans.
• Perform ongoing reviews of medical data.

Key requirements

• MD with clinical training; 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.
• Pharma/CRO industry or clinical development exposure is desirable (medical/project management or pharmacovigilance).
• Understanding of ICH-GCP and relevant regulations/guidance.
• Ideally prior experience as a medical monitor.
• Ideally experience with data visualization systems and IT systems.
• Clinical development/trials experience is an asset.

• ICH-GCP knowledge
• data visualization systems and IT systems
• medical monitoring
• clinical trial data review

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