Pharmaceutical Physician - London-based

Medpace

Pharmaceutical Research Industry

20095 Milanino, Lombardia - Italien

Senior Specialist / Project Manager

Experteer Overview

In this role you will provide medical, scientific, and strategic leadership for planning, executing, and reporting clinical trials. You will act as Medpace's internal medical expert, guiding interpretation of results in study reports and regulatory documents. You will help shape new clinical projects, including study design and protocols, across multiple therapeutic areas. This position offers hybrid WFH flexibility and an opportunity to impact trials across oncology, neurology, psychiatry, hepatology, dermatology, and metabolic diseases.

Compensation / Benefits

Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives

Responsibilities

Provide medical management and expertise for clinical trials
Contribute medical input to study reports, regulatory documents, and manuscripts
Manage safety issues in clinical trials and collaborate on evaluation of trials
Participate in new business development through proposal and sponsor meetings
Coordinate with other departments across all study phases (feasibility, design, medical information, and document review)
Lead adherence to research-related protocols and policies

Key requirements

MD degree or equivalent
Board certification and current medical licensure preferred
Prior clinical trial research experience
Previous experience in pharmaceutical-related clinical research preferred

strong communication and collaboration cross-functional coordination leadership and team orientation clinical trial management regulatory documentation and manuscripts safety assessment and pharmacovigilance

Description

In this role you will provide medical, scientific, and strategic leadership for planning, executing, and reporting clinical trials. You will…

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