Hepatology - Medical Director

Medpace; Lyon; Sur place; EUR 125 000 - 150 000; Plein temps

Résumé du poste

A leading clinical research organization in Lyon is seeking a Hepatologist to join their team. The Medical Director will provide medical and strategic leadership for clinical trials, ensuring adherence to protocols and collaboration across departments. Required qualifications include an M.D. in Hepatology and board certification. Experience in clinical trial research is preferred. This role also offers a hybrid work-from-home flexibility.

Qualifications

• Must have an M.D., specialization in Hepatology and current medical licensure.
• Board certification is required.
• Prior clinical trial research experience preferred.
• Previous experience in pharmaceutical-related clinical research is preferred.

Responsabilités

• Provide medical management and expertise for clinical trials.
• Contribute medical expertise to study reports, regulatory documents, and manuscripts.
• Manage safety issues in clinical trials and work closely with associates.
• Participate in new business development through involvement in proposal and sponsor meetings.
• Coordinate with other departments in all phases of the studies and trials.
• Follow specific research related protocol and lead others in adherence to the policies.

Description du poste

Overview

We are seeking a Hepatologist to join our team in London. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required.

All Medical Monitors have hybrid WFH flexibility.

Responsibilities

• Provide medical management and expertise for clinical trials;


• Contribute medical expertise to study reports, regulatory documents, and manuscripts;


• Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;


• Participate in new business development through involvement in proposal and sponsor meetings as requested;


• Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;


• Follow specific research related protocol and lead others in strict adherence to the policies.

Qualifications

• Must have an M.D., specialization in Hepatology and current medical licensure;


• Board certification;


• Prior clinical trial research experience preferred;


• Previous experience in pharmaceutical-related clinical research is preferred.

Travel

Up to 20%

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.