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For Companies At a Glance
- Tasks: Lead a global team to evaluate and support clinical trial opportunities.
- Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics.
- Benefits: Enjoy flexible work, competitive pay, generous PTO, and career growth opportunities.
- Why this job: Make a real impact on patients' lives while working in a dynamic, supportive environment.
- Qualifications: Bachelor's degree required; 5-7 years in clinical trial management preferred.
- Other info: Join a company recognised by Forbes for success and excellence in the industry.
The predicted salary is between 54000 - 84000 £ per year.
Responsibilities
We are currently seeking a Director, Feasibility , who will be an integral team leader within our global Proposals and Feasibility team. This position will evaluate and support new clinical trial opportunities by working strategically with Medpace Medical Experts, Clinical Trial Managers and our Regulatory Submissions team. By collaborating with Investigators and international country managers, as well as analysis of multiple data sources, this individual will strategize the most efficient scenario to conduct various studies globally. If you are an individual with a strong clinical background and expertise in clinical trial management, please review the following career opportunity.
Qualifications
- Bachelors required, Masters/PhD preferred
- 5-7years of project management/clinical trial management/feasibility experience in clinical research, CRO experienced preferred
- Analytical thinker with great attention to detail
- Thorough knowledge of feasibility processes
- Advanced understanding of operational aspects of clinical trials
- Ability to work independently
- Outstanding leadership, and communication skills
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 4,000 people across almost 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
- Bachelors required, Masters/PhD preferred
- 5-7years of project management/clinical trial management/feasibility experience in clinical research, CRO experienced preferred
- Analytical thinker with great attention to detail
- Thorough knowledge of feasibility processes
- Advanced understanding of operational aspects of clinical trials
- Ability to work independently
- Outstanding leadership, and communication skills
We are currently seeking a Director, Feasibility , who will be an integral team leader within our global Proposals and Feasibility team. This position will evaluate and support new clinical trial opportunities by working strategically with Medpace Medical Experts, Clinical Trial Managers and our Regulatory Submissions team. By collaborating with Investigators and international country managers, as well as analysis of multiple data sources, this individual will strategize the most efficient scenario to conduct various studies globally. If you are an individual with a strong clinical background and expertise in clinical trial management, please review the following career opportunity.
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Director, Feasibility (London) employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director, Feasibility (London)
✨Tip Number 1
Network with professionals in the clinical research field, especially those who have experience with CROs. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends in feasibility studies.
✨Tip Number 2
Familiarise yourself with Medpace's recent projects and case studies. Understanding their approach and success stories can help you tailor your discussions during interviews and demonstrate your genuine interest in their work.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences that highlight your analytical thinking and leadership skills. Be ready to explain how you've successfully managed clinical trials or feasibility studies in the past.
✨Tip Number 4
Stay updated on regulatory changes and advancements in clinical trial methodologies. Showing that you are proactive about your professional development will impress hiring managers and demonstrate your commitment to the field.
We think you need these skills to ace Director, Feasibility (London)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your project management and clinical trial management experience. Emphasise any relevant roles that demonstrate your analytical thinking and attention to detail, as these are key qualifications for the Director, Feasibility position.
Craft a Compelling Cover Letter: In your cover letter, express your passion for clinical research and your understanding of feasibility processes. Mention specific examples from your past experiences that showcase your leadership skills and ability to work independently.
Highlight Relevant Qualifications: Clearly state your educational background, especially if you have a Master's or PhD. Also, outline your years of experience in clinical research and any specific knowledge of operational aspects of clinical trials that would make you a strong candidate.
Showcase Collaborative Experience: Since the role involves collaboration with various teams, include examples of how you've successfully worked with cross-functional teams in the past. This could involve working with medical experts, regulatory submissions teams, or international managers.
How to prepare for a job interview at Medpace
✨Showcase Your Clinical Expertise
Make sure to highlight your clinical background and any relevant experience in clinical trial management. Be prepared to discuss specific projects you've led and the outcomes achieved, as this will demonstrate your capability to handle the responsibilities of the Director, Feasibility role.
✨Demonstrate Analytical Thinking
Since the role requires an analytical thinker with great attention to detail, prepare examples of how you've approached complex problems in previous roles. Discuss how you analysed data sources to make informed decisions, which is crucial for strategising efficient study scenarios.
✨Emphasise Leadership Skills
As a team leader, it's important to convey your leadership style and how you've successfully managed teams in the past. Share experiences where you motivated your team or resolved conflicts, showcasing your outstanding communication skills.
✨Understand the Company’s Mission
Familiarise yourself with Medpace's mission and values. Be ready to discuss how your personal goals align with their purpose of improving lives through clinical research. This shows your genuine interest in the company and its impact on global health.
