Therapeutic Area Medical Director

Medpace; München; Hybrid; EUR 90.000 - 130.000; Vollzeit

Benefits dieser Stelle

Flexible work environment

Competitive compensation and benefits package

Structured career paths with opportunities for professional growth

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Zusammenfassung

A clinical research organization seeks several Medical Directors in Munich, Germany. The role involves providing medical and strategic leadership in clinical trials, managing clinical trial safety, contributing to study reports, and coordinating with departments. Candidates should hold an M.D. or equivalent, with clinical trial experience preferred. The position offers a flexible hybrid work environment and a competitive benefits package for professional growth.

Qualifikationen

• M.D. degree or equivalent with board certification preferred.
• Prior clinical trial research experience is essential.
• Experience in pharmaceutical-related clinical research is preferred.

Aufgaben

• Provide medical management and expertise for clinical trials.
• Contribute medical expertise to study reports and regulatory documents.
• Manage safety issues in clinical trials.

Kenntnisse

Clinical trial management

Medical expertise

Safety assessment

Team coordination

Ausbildung

M.D. degree or equivalent

Board certification preferred

Jobbeschreibung

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

All Medical Directors have hybrid WFH flexibility.

The following Therapeutic Areas

• Psychiatry
• Rare Disease / Pediatrics
• Neurology
• Oncology (solid tumor)
• Hematology
• Hepatology
• Dermatology
• Metabolic / Endocrinology
• Pulmonology

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. degree or equivalent. Board certification and current medical licensure are preferred;
• Must have prior clinical trial research experience; and
• Previous experience in pharmaceutical-related clinical research is preferred.

Travel

Up to 20%.

Perks

• 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