Dermatology Medical Director — Remote Clinical Trials Leader

Medpace; Vlaams-Brabant; Hybrid; EUR 120,000 - 180,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits

Competitive PTO packages

Structured career paths with growth

Company-sponsored employee events

Employee health and wellness

Job summary

Medpace in Belgium (Vlaams-Brabant) seeks Medical Directors to provide medical, scientific, and strategic leadership for planning, execution, and reporting of clinical trials. Serve as the internal medical expert for study design, protocols, and project plans.

Responsibilities include medical management, safety oversight, and collaboration across departments; travel up to 20% and involvement in sponsor meetings as needed.

Qualifications

• Must have an M.D. degree or equivalent.
• Board certification and current medical licensure are preferred.
• Must have prior clinical trial research experience.
• 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 degree

Board certification (preferred)

Medical licensure (preferred)

Clinical trial research experience

Pharmaceutical-related clinical research experience (preferred)

Job description

Medpace in Belgium (Vlaams-Brabant) seeks Medical Directors to provide medical, scientific, and strategic leadership for planning, execution, and reporting of clinical trials. Serve as the internal medical expert for study design, protocols, and project plans.

Responsibilities include medical management, safety oversight, and collaboration across departments; travel up to 20% and involvement in sponsor meetings as needed.