Therapeutic Area Medical Director — Hybrid/Remote Leader

Medpace; Cincinnati (OH); Hybrid; GBP 150,000 - 210,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits

Competitive PTO packages

Structured career paths

Company-sponsored employee recognition

Employee health and wellness

Job summary

Medpace is seeking a Therapeutic Area Medical Director to provide medical, scientific, and strategic leadership for global clinical trials. The role includes study design input, safety oversight, and collaboration with sponsor teams to deliver high-quality clinical study reports.

The ideal candidate holds an MD with board certification and extensive experience in pharmaceutical-related clinical research, and is comfortable with hybrid working arrangements in the UK.

Qualifications

• Must have an MD degree or equivalent.
• Board certification and current medical licensure are preferred.
• Must have prior clinical trial research experience; and
• Previous experience in pharmaceutical-related clinical research is preferred.
• Travel: up to 20%

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.

Skills

Medical leadership

Clinical trial experience

Education

MD degree

Board certification

Medical licensure

Job description

Medpace is seeking a Therapeutic Area Medical Director to provide medical, scientific, and strategic leadership for global clinical trials. The role includes study design input, safety oversight, and collaboration with sponsor teams to deliver high-quality clinical study reports.

The ideal candidate holds an MD with board certification and extensive experience in pharmaceutical-related clinical research, and is comfortable with hybrid working arrangements in the UK.