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For Companies At a Glance
- 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 with impactful work in healthcare innovation.
- 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.
Job Summary
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.
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Associate Clinical Trial Manager (PhD) - Infectious Disease / Immunology employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Trial Manager (PhD) - Infectious Disease / Immunology
✨Tip Number 1
Familiarise yourself with the clinical trial process and the specific role of an Associate Clinical Trial Manager. Understanding the nuances of project management in a clinical setting will help you engage more effectively during interviews.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who have transitioned from academia to industry. They can provide valuable insights and may even refer you to opportunities at Medpace.
✨Tip Number 3
Prepare to discuss your analytical skills and how they can be applied to clinical project management. Be ready to give examples from your PhD or post-doctoral research that demonstrate your ability to manage complex data and projects.
✨Tip Number 4
Show enthusiasm for the therapeutic areas Medpace focuses on, such as infectious diseases and immunology. Research recent developments in these fields to demonstrate your genuine interest and commitment during your interactions with the team.
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 from your academic background that demonstrate your suitability for the role.
Highlight Relevant Skills: In your application, focus on skills that are crucial for the Associate Clinical Trial Manager position, such as communication, collaboration, and attention to detail. Provide examples of how you've used these skills in your previous work or research.
Prepare for Potential Questions: Anticipate questions related to your research experience and how it can be applied to clinical trial management. Be ready to discuss your understanding of the clinical trial process and your ability to work in a fast-paced environment.
How to prepare for a job interview at Medpace
✨Showcase Your Academic Background
As a PhD candidate, your academic achievements are crucial. Be prepared to discuss your research, methodologies, and how they relate to clinical trial management. Highlight any relevant projects that demonstrate your analytical skills.
✨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, whether in presentations or team discussions.
✨Familiarise Yourself with Clinical Trial Processes
Even if you lack direct experience in the CRO or pharmaceutical industry, understanding the basics of clinical trials will set you apart. Research common terminologies and processes to show your enthusiasm and readiness to learn.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities in dynamic environments. Think of scenarios where you had to manage multiple tasks or resolve conflicts, and be ready to explain your thought process and outcomes.
