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- Tasks: Lead clinical trials and provide medical expertise in various therapeutic areas.
- Company: Medpace is a global leader in clinical research, impacting patient lives through innovative therapies.
- Benefits: Enjoy flexible work options, competitive pay, and structured career growth opportunities.
- Why this job: Make a real difference in healthcare while working with a passionate team dedicated to innovation.
- Qualifications: Must have an M.D., board certification, and prior clinical trial research experience.
- Other info: Hybrid work flexibility available; travel up to 20% may be required.
The predicted salary is between 72000 - 108000 £ per year.
Job Summary:
We are seeking a 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 the following Therapeutic Areas:
- Oncology (adult)
- Cardiology (adult)
- Gastroenterology
- Endocrinology
- Radiology
- Infectious Disease
- Immunology
- Nephrology
- Neurology
- Psychiatrist
We are open to various locations throughout Europe.
All Medical Directors have hybrid WFH flexibility. This role also has the ability to be fully remote with the right experience.
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. with board certification and current medical licensure;
- Must have prior clinical trial research experience;
- 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 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.
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
What to Expect Next:
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
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Medical Director - Oncology/Cardiology/Gastroenterology/Endocrinology/Radiology/Infectious Dise[...] employer: Medpace, Inc.
Contact Detail:
Medpace, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Director - Oncology/Cardiology/Gastroenterology/Endocrinology/Radiology/Infectious Dise[...]
✨Tip Number 1
Make sure to highlight your clinical trial research experience during the interview. Be prepared to discuss specific trials you've worked on, your role in them, and how you contributed to their success.
✨Tip Number 2
Familiarize yourself with Medpace's mission and values. Understanding their approach to clinical development will help you align your answers with their goals and demonstrate your commitment to making a difference.
✨Tip Number 3
Network with current or former Medpace employees if possible. They can provide valuable insights into the company culture and expectations for the Medical Director role, which can help you tailor your responses.
✨Tip Number 4
Prepare to discuss your experience with safety issues in clinical trials. Be ready to share examples of how you've managed these challenges and collaborated with teams to ensure compliance and patient safety.
We think you need these skills to ace Medical Director - Oncology/Cardiology/Gastroenterology/Endocrinology/Radiology/Infectious Dise[...]
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your clinical trial research experience and any relevant therapeutic area expertise in your application. This will demonstrate your suitability for the Medical Director role.
Tailor Your CV: Customize your CV to reflect the specific qualifications and responsibilities mentioned in the job description. Include details about your medical management experience and any contributions to study reports or regulatory documents.
Craft a Strong Cover Letter: Write a compelling cover letter that outlines your passion for clinical research and how your background aligns with Medpace's mission. Mention your board certification and current medical licensure to strengthen your application.
Prepare for Potential Interviews: Anticipate questions related to your experience in managing clinical trials and your approach to safety issues. Be ready to discuss your involvement in study design and protocol development, as these are key aspects of the role.
How to prepare for a job interview at Medpace, Inc.
✨Showcase Your Medical Expertise
As a Medical Director, it's crucial to demonstrate your deep understanding of clinical trials and therapeutic areas. Be prepared to discuss your previous experiences in clinical research and how they relate to the responsibilities outlined in the job description.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about past challenges you've faced in clinical trials and how you managed safety issues or coordinated with other departments.
✨Highlight Your Leadership Skills
This role requires strong leadership capabilities. Be ready to share examples of how you've led teams or projects in the past, particularly in the context of medical management and strategic planning.
✨Understand Medpace's Mission and Values
Familiarize yourself with Medpace's mission to accelerate the development of safe and effective medical therapeutics. Show your alignment with their values by discussing how your work can contribute to improving patient lives.
