Hematologist - Medical Director
Medpace, City of London
Hematologist - Medical Director
Salary not available. View on company website.
Medpace, City of London
- Full time
- Permanent
- Remote working
Posted 2 weeks ago, 30 Aug | Get your application in now before you miss out!
Closing date: Closing date not specified
Job ref: ee195058bc954918a109f503d2a770bf
Location ref: City of London
Full Job Description
Hematologist - Medical Director
Date: 2026-08-28
Location: City of London, Greater London, GB, EC4N 6JD
Application Deadline: 2026-11-26T09:04:12.12
Job Summary
We are seeking a Hematologist Medical Director 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. We are currently seeking Medical Directors in different locations. All Medical Directors have hybrid WFH flexibility.
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. degree or equivalent. Board certification and current medical licensure are preferred;
- Prior clinical trial research experience preferred;
- Previous experience in pharmaceutical-related clinical research is preferred.
Travel
Up to 20%
Benefits
- Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
#s1-Gen
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. degree or equivalent. Board certification and current medical licensure are preferred; Prior clinical trial research experience preferred; and Previous experience in pharmaceutical-related clinical research is preferred. Travel: up to 20% Benefits Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives
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