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- Tasks: Join our team to manage clinical trials and collaborate on global study activities.
- Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics.
- Benefits: Enjoy flexible work, competitive pay, professional growth opportunities, and wellness initiatives.
- Why this job: Kickstart your career in a dynamic environment while making a real impact on patients' lives.
- Qualifications: PhD in Life Sciences and strong English presentation skills required; prior industry experience is a plus.
- Other info: Intensive training provided for recent graduates aiming for rapid career advancement.
The predicted salary is between 36000 - 60000 £ per year.
Medpace is currently seeking candidates with Cardiovascular related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).
Responsibilities
- Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
- Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
- Compile and maintain project-specific status reports within the clinical trial management system
- Interact with the internal project team, Sponsor, study sites, and third-party vendors
- Provide oversight and quality control of our internal regulatory filing system
- Provide oversight and management of study supplies
- Create and maintain project timelines
- Coordinate project meetings and produce quality minutes
Qualifications
- PhD in Life Sciences
- Fluency in English with solid presentation skills
- Ability to work in a fast-paced dynamic industry within an international team
- Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
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.
Associate Clinical Trial Manager (PhD) - Cardiovascular employer: Medpace, Inc.
Contact Detail:
Medpace, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Trial Manager (PhD) - Cardiovascular
✨Tip Number 1
Network with professionals in the clinical trial management field, especially those who have experience in cardiovascular research. Attend industry conferences or webinars to connect with potential colleagues and learn more about the role.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical trials, particularly in the cardiovascular sector. This knowledge will not only boost your confidence but also demonstrate your commitment to the field during interviews.
✨Tip Number 3
Prepare to discuss how your PhD research can be applied to clinical trial management. Think of specific examples where your analytical skills and academic background can contribute to the success of clinical projects.
✨Tip Number 4
Show enthusiasm for the role and the company during any interactions. Medpace values passion and purpose, so expressing your desire to make a difference in the field of therapeutics can set you apart from other candidates.
We think you need these skills to ace Associate Clinical Trial Manager (PhD) - Cardiovascular
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your PhD in Life Sciences and any relevant research experience, especially in cardiovascular topics. Use keywords from the job description to demonstrate your fit for the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical trial management and your analytical skills. Mention specific experiences from your PhD that relate to the responsibilities of the Associate Clinical Trial Manager position.
Highlight Communication Skills: Since the role involves collaboration with various stakeholders, emphasise your communication and presentation skills. Provide examples of how you've effectively communicated complex information during your academic career.
Show Enthusiasm for the Role: In your application, express your eagerness to transition into the clinical trial management field. Discuss your desire for professional growth and how you see yourself contributing to Medpace's mission.
How to prepare for a job interview at Medpace, Inc.
✨Showcase Your Academic Background
As a candidate with a PhD in Life Sciences, make sure to highlight your research experience and how it relates to clinical trial management. Be prepared to discuss specific projects you've worked on and the analytical skills you've developed.
✨Demonstrate Communication Skills
Since the role involves collaboration with various stakeholders, practice articulating your thoughts clearly. Prepare examples of how you've effectively communicated complex information in past experiences, especially in a team setting.
✨Familiarise Yourself with Clinical Trial Processes
Even if you don't have direct experience in the CRO or pharmaceutical industry, showing a solid understanding of clinical trial phases and management processes can set you apart. Research Medpace's approach and be ready to discuss how you can contribute.
✨Express Your Desire for Growth
Medpace values candidates who are eager to learn and grow within the company. Be honest about your career aspirations and how this position aligns with your long-term goals in clinical trial management.
