Clinical Research Medical Leader

2 weeks ago


Bristol, Maine, United States Medpace Full time
Position Overview:

We are looking for a Medical Director to become a vital part of our innovative team. This role encompasses the overall responsibility for delivering medical, scientific, and strategic guidance for the effective planning, execution, and reporting of clinical studies. The Medical Director will also serve as the internal medical authority at Medpace, providing essential medical insights for the evaluation, presentation, and interpretation of findings in the Clinical Study Report. Furthermore, this position will engage in the formulation of new clinical initiatives, including study design, protocol development, and project planning as necessary. We are actively seeking Medical Directors across various Therapeutic Areas:

  • Endocrinology
  • Lipidology
  • CNS
  • Nephrology
  • Immunology
  • Rheumatology
  • Metabolic Disease
  • Oncology / Hematology
  • Cardiovascular
Key Responsibilities:
  • Overseeing and monitoring clinical trials with medical expertise;
  • Engaging in business development through participation in proposal and sponsor discussions as needed;
  • Providing medical and scientific knowledge, contributing to study reports, regulatory documents, and publications;
  • Addressing safety concerns in clinical trials by collaborating closely with team members to evaluate and assess the trials;
  • Collaborating in cross-functional teams throughout all phases of studies and trials, including feasibility assessments, design processes, educational initiatives, management of medical information, and reviewing and editing medical documentation.
Qualifications:
  • Doctor of Medicine degree;
  • Active medical license (not restricted to a specific country);
  • Board certification in the relevant area of expertise;
  • Prior experience in clinical trial research is essential;
  • Experience in pharmaceutical-related clinical research is preferred.

Travel Requirements: Up to 20%

About Medpace:

Medpace is a comprehensive clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device sectors. Our mission is to expedite the global development of safe and effective medical therapies through a scientific and disciplined approach. We utilize local regulatory and therapeutic expertise across all major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. We employ over 5,000 professionals across more than 40 countries.

Why Choose Medpace?

At Medpace, we value People, Purpose, and Passion. Our work over the past three decades has positively influenced the lives of numerous patients and families facing various diseases across all key therapeutic areas. The contributions we make today will enhance the lives of individuals dealing with illness and disease in the future.

Medpace Benefits:
  • Hybrid work-from-home options (dependent on position and level);
  • Competitive PTO packages;
  • Company-sponsored employee appreciation events;
  • Health and wellness initiatives for employees;
  • Flexible work schedules;
  • Attractive compensation and benefits package;
  • Structured career paths with opportunities for professional advancement.
Awards and Recognition:
  • Recognized by Forbes as one of America's Most Successful Midsize Companies in recent years;
  • Consistently awarded CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
Next Steps:

A member of the Medpace team will review your qualifications, and if there is mutual interest, you will be contacted with further details regarding the next steps.

Medpace is an EO/AA Employer M/F/Disability/Vets.



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