Clinical Research Psychiatrist

Medpace; Cincinnati (OH); Hybrid; GBP 70,000 - 110,000; Full time

Benefits offered by this job

Hybrid work flexibility

Competitive compensation package

Job summary

Medpace is seeking a Psychiatry Medical Monitor to provide medical, scientific, and strategic leadership for planning, execution, and reporting of clinical trials. You will serve as the internal medical expert for study interpretation and contribute to protocol and project plans.

The role offers hybrid WFH flexibility and involves travel up to 20%. The position uses your MD-level expertise to support regulatory documents, manuscripts, and new business development.

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%

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 with teams on evaluation and assessment.
• Participate in new business development through sponsor meetings and proposals.
• Coordinate with departments across feasibility, design, medical information, and document review.
• Follow research protocols and lead others in adherence to policies.

Education

MD or equivalent

Board certification

Medical licensure

Job description

We are seeking a psychiatry Medical Monitor to join our dynamic team. The Medical Monitor 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 Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required.

All Medical Monitors 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;
• and Previous experience in pharmaceutical-related clinical research is preferred.
• Travel: up to 20%

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

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
• Awards
• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility