Remote Medical Director, Endocrine/Metabolic Trials

Medpace; Cincinnati (OH); Hybrid; USD 190,000 - 260,000; Full time

Benefits offered by this job

Flexible work environment

Comprehensive PTO

Competitive compensation package

Employee health and wellness programs

Career development opportunities

Company-sponsored events

Job summary

Medpace in Cincinnati, OH seeks a Medical Director in Endocrine/Metabolic Disease to provide medical, scientific, and strategic leadership for clinical trials. You will support study design, protocol development, and reporting, with internal medical expert responsibilities across therapeutic areas.

The role offers hybrid work-from-home flexibility and the possibility of full remote work with the right experience, supporting cross-functional collaboration and ongoing medical oversight.

Qualifications

• Must have an M.D., specialization in Endocrine/Metabolic Disease.
• 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.

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.

Education

MD, Endocrine/Metabolic Disease

Job description

Medpace in Cincinnati, OH seeks a Medical Director in Endocrine/Metabolic Disease to provide medical, scientific, and strategic leadership for clinical trials. You will support study design, protocol development, and reporting, with internal medical expert responsibilities across therapeutic areas.

The role offers hybrid work-from-home flexibility and the possibility of full remote work with the right experience, supporting cross-functional collaboration and ongoing medical oversight.