Medical Director
2 days ago
We are seeking a Medical Director to join our dynamic team in the Clinical Pharmacology Unit (CPU). This Medical Director will have overall responsibility for overseeing the conduct of clinical trials in the CPU as Principal Investigator. Furthermore, they will be providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of phase 1 clinical trials. Additionally, this role acts as the Medpace internal medical expert and may serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director may also be involved in the development of new clinical projects, including study design and protocol plans as required.
As Principal Investigator in the CPU, this physician will follow FDA and GCP guidance:
"In conducting clinical investigations of drugs, including biological products, under 21 CFR part 312 and of medical devices under 21 CFR part 812, the investigator is responsible for:
- Ensuring that a clinical investigation is conducted according to the signed investigator statement for clinical investigations of drugs, including biological products, or agreement for clinical investigations of medical devices, the investigational plan, and applicable regulations
- Protecting the rights, safety, and welfare of subjects under the investigator's care
- Controlling drugs, biological products, and devices under investigation (21 CFR 312.60, 21 CFR 812.100)"
- Provide medical oversight of clinical trials as Principal Investigator, including training of staff as necessary
- Decides on eligibility of subjects for participation in clinical trials
- Safeguards the well being of subjects during any clinical trial
- Provides medical care as needed during conduct of clinical trial
- Contributes as PI to study reports, regulatory documents, and manuscripts;
- Manage safety issues in clinical trials, report issues timely, and work closely with associates in evaluation and assessment of the trials;
- Follow specific research related protocol and lead others in strict adherence to the policies.
- Participate in new business development through involvement in proposal and sponsor meetings as requested;
- Must have an M.D. or D.O. with current medical licensure; board certification is desirable
- Previous experience in pharmaceutical-related clinical research is preferred.
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 5,000 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.
Cincinnati Perks
- Cincinnati Campus Overview
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with local nonprofit organizations
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Structured career paths with opportunities for professional growth
- Discounted tuition for UC online programs
- Named a Top Workplace in 2024 by The Cincinnati Enquirer
- 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
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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