Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead clinical trials and provide medical expertise in oncology.
- Company: Medpace is a global leader in clinical research, impacting patient lives through innovative therapies.
- Benefits: Enjoy hybrid work flexibility, competitive pay, and structured career growth opportunities.
- Why this job: Join a passionate team making a real difference in healthcare and patient outcomes.
- Qualifications: Must have an M.D. in Oncology, board certification, and clinical trial experience preferred.
- Other info: Travel up to 20% may be required; fully remote options available for experienced candidates.
The predicted salary is between 43200 - 72000 £ per year.
Job Summary
We are seeking Oncologists – Medical Directors 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 different locations.
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., specialization in Oncology and current medical licensure;
- Board certification;
- 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 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
#J-18808-Ljbffr
Oncologist - Medical Director employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Oncologist - Medical Director
✨Tip Number 1
Familiarize yourself with the latest advancements in oncology and clinical trial methodologies. This knowledge will not only help you during interviews but also demonstrate your commitment to staying at the forefront of the field.
✨Tip Number 2
Network with professionals in the oncology and clinical research fields. Attend relevant conferences or webinars to connect with potential colleagues and learn more about Medpace's work culture and values.
✨Tip Number 3
Prepare to discuss your previous experiences in clinical trials, especially any leadership roles you've held. Highlight specific examples where you contributed to study design or managed safety issues effectively.
✨Tip Number 4
Research Medpace’s recent projects and publications in oncology. Being knowledgeable about their work will allow you to ask insightful questions during the interview and show your genuine interest in joining their team.
We think you need these skills to ace Oncologist - Medical Director
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your clinical trial research experience and any previous work in pharmaceutical-related clinical research. This will show that you have the necessary background for the Medical Director role.
Tailor Your CV: Customize your CV to reflect the qualifications listed in the job description, such as your M.D., specialization in Oncology, and board certification. Include specific examples of your leadership in clinical trials.
Craft a Strong Cover Letter: Write a compelling cover letter that outlines your passion for oncology and your vision for contributing to Medpace's mission. Mention how your expertise aligns with their goals and the impact you hope to make.
Prepare for Interviews: If selected for an interview, be ready to discuss your medical management strategies for clinical trials and how you handle safety issues. Prepare to share insights on study design and protocol development.
How to prepare for a job interview at Medpace
✨Showcase Your Medical Expertise
As a Medical Director, your medical knowledge is crucial. Be prepared to discuss your experience in oncology and clinical trials in detail. Highlight specific cases where you provided leadership or made significant contributions.
✨Demonstrate Strategic Thinking
The role requires strategic leadership for clinical trials. Prepare examples of how you've successfully planned and executed clinical projects, including study design and protocol development. This will show your ability to think critically and strategically.
✨Emphasize Collaboration Skills
Collaboration with various departments is key in this role. Share experiences where you worked cross-functionally, managed safety issues, or coordinated with other teams. This will illustrate your ability to work well in a team-oriented environment.
✨Prepare for Regulatory Discussions
Since the position involves contributing to regulatory documents and study reports, familiarize yourself with relevant regulations and guidelines. Be ready to discuss how you've navigated these in past roles, showcasing your understanding of compliance and quality assurance.
