Medpace

Psychiatrist - Medical Director

Medpace$180K — $220K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • M.D. with a specialization in Psychiatry
  • Eligible for obtaining a medical license
  • Board certification preferred
  • Prior clinical trial research experience preferred
  • Experience in pharmaceutical-related clinical research preferred

Responsibilities

  • Provide medical management and expertise for clinical trials
  • Contribute medical expertise to study reports and regulatory documents
  • Manage safety issues and collaborate on evaluation of trials
  • Participate in business development through proposal and sponsor meetings
  • Coordinate with departments on study phases and review medical documents
  • Lead adherence to research protocols among team members

Benefits

  • Hybrid work environment with the option for fully remote work
  • Competitive PTO starting at 20+ days
  • Comprehensive compensation and benefits package
  • Employee appreciation events and wellness initiatives
  • Community involvement opportunities
  • On-site fitness center at a modern campus
  • Structured career paths and professional growth opportunities
  • Discounted tuition for UC online programs
Full Job Description
Job Summary

We are seeking a Medical Director in Psychiatry to join our dynamic team in Cincinnati, Ohio. The Medical Director has 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. We are currently seeking Medical Directors in all Therapeutic Areas.

*All Medical Directors receive hybrid, work from-home flexibility. This role also has the ability to be fully remote-based 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., specialization in Psychiatry
  • 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% at times

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.

About Medpace

Medpace is a clinical research organization that provides services to pharmaceutical, biotechnology, and medical device companies. The company's services include clinical trial management, regulatory consulting, and medical imaging. Medpace was founded in 1992 and is headquartered in Cincinnati, Ohio. The company has operations in North America, Europe, and Asia.
Learn more about Medpace
Size
4,700 employees
Market Cap
$6.4 billion
Industry
Net Income
$145.3 million
Founded
1992
5 Year Trend
+22.1%
Revenue
$925.9 million
NASDAQ

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