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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 difference in 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 28800 - 48000 £ 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.
- Manage and perform 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) - Infectious Disease / Immunology 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) - Infectious Disease / Immunology
✨Tip Number 1
Network with professionals in the clinical trial management field. Attend industry conferences or webinars where you can meet people from Medpace or similar organisations. Building these connections can give you insights into the company culture and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest trends and technologies in clinical trial management. Being knowledgeable about current practices will not only boost your confidence but also demonstrate your commitment to the role during interviews.
✨Tip Number 3
Prepare to discuss how your PhD research can be applied to clinical project management. Think of specific examples where you've demonstrated analytical skills, teamwork, or problem-solving that are relevant to the responsibilities of an Associate Clinical Trial Manager.
✨Tip Number 4
Show enthusiasm for the role and the impact of clinical trials on patient lives. During any interactions with Medpace, express your passion for contributing to the development of therapeutics and how you see yourself growing within the company.
We think you need these skills to ace Associate Clinical Trial Manager (PhD) - Infectious Disease / Immunology
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 clinical research and your desire to transition into the industry. Mention specific experiences that demonstrate your ability to work in a fast-paced environment and collaborate with teams.
Highlight Relevant Skills: In your application, focus on skills that are crucial for the role, such as communication, organisation, and attention to detail. Provide examples of how you've used these skills in your academic or research work.
Prepare for Potential Interviews: While this step is not part of the written application, it's good to prepare for interviews by thinking about how you can discuss your research experience and its relevance to clinical trial management. Be ready to explain your motivation for joining Medpace and how you can contribute to their mission.
How to prepare for a job interview at Medpace, Inc.
✨Showcase Your Academic Background
As a candidate with a PhD, it's crucial 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 an international context.
✨Understand the Clinical Trial Process
Familiarise yourself with the basics of clinical trial management and the role of an Associate Clinical Trial Manager. This knowledge will help you answer questions confidently and show your enthusiasm for the position.
✨Prepare for Scenario-Based Questions
Expect to face scenario-based questions that assess your problem-solving abilities and decision-making skills. Think of examples from your academic or research background where you had to manage timelines, coordinate teams, or ensure quality control.
