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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 making a real impact on patient lives.
- Qualifications: PhD in Life Sciences and strong English presentation skills required.
- 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 PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our 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) - Oncology 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) - Oncology
✨Tip Number 1
Network with professionals in the clinical trial management field, especially those who have experience in oncology. Attend industry conferences or webinars to meet potential colleagues and learn more about the role.
✨Tip Number 2
Familiarise yourself with clinical trial management systems and tools commonly used in the industry. This knowledge will not only boost your confidence but also demonstrate your proactive approach to learning.
✨Tip Number 3
Prepare to discuss your PhD research and how it relates to clinical trials during interviews. Highlight any relevant analytical skills or experiences that can be applied to project management.
✨Tip Number 4
Show enthusiasm for the role and the company’s mission. Research Medpace’s recent projects and achievements in oncology to express genuine interest and align your goals with theirs.
We think you need these skills to ace Associate Clinical Trial Manager (PhD) - Oncology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your PhD and any relevant research experience. Emphasise skills that align with clinical trial management, such as analytical abilities and project coordination.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for oncology and clinical trials. Mention specific experiences that demonstrate your ability to work in a fast-paced environment and your desire to grow within the industry.
Highlight Relevant Skills: In your application, focus on skills that are crucial for the role, such as communication, collaboration, and attention to detail. Provide examples of how you've used these skills in your academic or research work.
Prepare for Potential Questions: Think about questions you might be asked during an interview, such as your understanding of clinical trial processes or how you handle tight deadlines. Prepare thoughtful responses that reflect your knowledge and enthusiasm for the role.
How to prepare for a job interview at Medpace, Inc.
✨Showcase Your Analytical Skills
As a candidate with a PhD, it's crucial to highlight your analytical and academic skills during the interview. Be prepared to discuss specific examples from your research that demonstrate your ability to analyse data and solve complex problems, as these skills are essential for the Associate Clinical Trial Manager role.
✨Understand the Clinical Trial Process
Familiarise yourself with the clinical trial management process, especially in oncology. Research Medpace's approach and be ready to discuss how your background can contribute to their mission of developing safe and effective therapeutics. This shows your genuine interest in the role and the company.
✨Prepare for Team Collaboration Questions
Since the role involves working closely with project coordinators and clinical trial managers, expect questions about teamwork and collaboration. Prepare examples of how you've successfully worked in teams during your academic career, focusing on communication and conflict resolution.
✨Ask Insightful Questions
At the end of the interview, take the opportunity to ask thoughtful questions about the company's projects, culture, and training programmes. This not only demonstrates your enthusiasm for the position but also helps you assess if Medpace is the right fit for you.
