Hepatology Clinical Trials Director

Medpace; Stirling; Hybrid; GBP 120,000 - 150,000; Full time

Job summary

Medpace in Stirling is seeking a Hepatologist Medical Director to provide medical, scientific, and strategic leadership for the planning, execution, and reporting of clinical trials. The Medical Director will serve as Medpace's internal medical expert and will aid in the review, presentation, and interpretation of results for Clinical Study Reports.

Travel up to 20% may be required. The role includes developing new clinical projects, study design, protocol, and project plans as required, with

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.

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.

Job description

Medpace in Stirling is seeking a Hepatologist Medical Director to provide medical, scientific, and strategic leadership for the planning, execution, and reporting of clinical trials. The Medical Director will serve as Medpace's internal medical expert and will aid in the review, presentation, and interpretation of results for Clinical Study Reports.

Travel up to 20% may be required. The role includes developing new clinical projects, study design, protocol, and project plans as required, with