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Medpace

Global CRO delivering full-service clinical trials

Therapeutic Area Medical Director

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeMunich, GermanyNo salary listed

About the Job

Requirements

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

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 protocols and lead others in strict adherence to the policies.
  • Provide medical, scientific, and strategic leadership for the planning, execution, and reporting of clinical trials.
  • Serve as Medpace's internal medical expert and resource for the review, presentation, and interpretation of results in the Clinical Study Report.
  • Contribute to development of new clinical projects, including study design, protocols, and project plans as required.

Desired Qualifications

  • Previous experience in pharmaceutical-related clinical research.
  • Board certification and current medical licensure.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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