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For Companies At a Glance
- Tasks: Lead clinical trials and provide medical expertise in various therapeutic areas.
- Company: Join Medpace, a top-tier clinical research organization making a global impact.
- Benefits: Enjoy flexible work options, competitive pay, and career growth opportunities.
- Why this job: Make a difference in patients' lives while working in a dynamic and supportive environment.
- Qualifications: Must have an M.D., board certification, and clinical trial research experience.
- Other info: Hybrid work flexibility with potential for fully remote roles.
The predicted salary is between 43200 - 72000 £ 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; 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 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
Contact Detail:
Medpace 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 networking opportunities. Connect with professionals in the industry through LinkedIn or relevant conferences, and discuss your background in clinical trials to showcase your expertise.
✨Tip Number 2
Familiarize yourself with Medpace's mission and values. Understanding their approach to clinical development will help you align your discussions and demonstrate how your experience can contribute to their goals.
✨Tip Number 3
Engage with current or former employees of Medpace to gain insights into the company culture and expectations for the Medical Director role. This can provide you with valuable information that can be used during interviews.
✨Tip Number 4
Stay updated on the latest trends and advancements in the therapeutic areas mentioned in the job description. Being knowledgeable about recent developments in oncology, cardiology, and other fields will position you as a strong candidate.
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. Tailor your CV to showcase your M.D. qualifications, board certification, and any specific projects you've led.
Craft a Strong Cover Letter: Write a compelling cover letter that outlines your passion for the role and how your background aligns with Medpace's mission. Discuss your leadership skills and how you can contribute to the planning and execution of clinical trials.
Demonstrate Medical Expertise: In your application, provide examples of how you've contributed medical expertise to study reports or regulatory documents in the past. This will show your capability to serve as a medical resource within the team.
Follow Application Instructions: Carefully read the job posting and follow all application instructions provided by Medpace. Ensure that you submit all required documents and that your application is complete before hitting 'submit' on our website.
How to prepare for a job interview at Medpace
✨Showcase Your Medical Expertise
As a Medical Director, you'll need 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 role.
✨Prepare for Technical Questions
Expect questions that assess your knowledge of study design, protocol development, and regulatory requirements. Brush up on recent advancements in oncology, cardiology, gastroenterology, and other relevant fields to showcase your expertise.
✨Highlight Leadership Skills
This role requires strong leadership abilities. Share examples of how you've successfully led teams in clinical settings, managed safety issues, or coordinated with various departments during trials.
✨Demonstrate Strategic Thinking
Be ready to discuss how you would approach new clinical projects and contribute to business development. Think about how you can align your medical expertise with the company's goals and mission.
