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Medical Director

Medpace, Inc.
Posted a month ago, valid for 11 days
Location

Cincinnati, OH, US

Salary

Competitive

Contract type

Full Time

Paid Time Off

By applying, a Medpace, Inc. account will be created for you. Medpace, Inc.'s Privacy Policy and Terms & Conditions will apply.

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Sonic Summary

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  • Medpace is seeking a Medical Director with clinical specialization in areas such as Gastroenterology, Neurology, and Cardiology to provide leadership for clinical trials.
  • The role requires an M.D. with therapeutic area specialization and prior clinical trial research experience preferred, along with eligibility to obtain a medical license.
  • Responsibilities include managing clinical trials, contributing medical expertise to study reports, and coordinating with various departments throughout the study phases.
  • The position offers hybrid work-from-home flexibility, with the possibility of being fully remote for candidates with the right experience.
  • Compensation is competitive, reflecting performance, with comprehensive health and wellness benefits included.

We are seeking a Medical Director with clinical specialization  (varying therapeutic areas including, but not limited to Gastroenterology/Hepatology, Neurology/Psychiatry, Nephrology, Cardiology, and more) 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. 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 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. This role also has the ability to be fully remote with the right experience**.


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., with a therapeutic area specialization 
  • Must be eligible to obtain a medical license
  • Board certification preferred
  • 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) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.


Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

 

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

 

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

 

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

 

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

 

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

 

 

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.




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By applying, a Medpace, Inc. account will be created for you. Medpace, Inc.'s Privacy Policy and Terms & Conditions will apply.

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