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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 with intensive training in a dynamic, international environment making a real impact.
- Qualifications: PhD in Life Sciences and strong English presentation skills required; prior industry experience is a plus.
- Other info: Recognised by Forbes as one of America's Most Successful Midsize Companies.
The predicted salary is between 28800 - 48000 £ per year.
Overview
Medpace is currently seeking candidates with Renal 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.
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Associate Clinical Trial Manager (PhD) - Renal employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Trial Manager (PhD) - Renal
✨Tip Number 1
Familiarise yourself with the latest trends and developments in renal research. This will not only enhance your understanding but also allow you to engage in meaningful conversations during interviews, showcasing your passion for the field.
✨Tip Number 2
Network with professionals in the clinical trial management space, especially those who have transitioned from academia to industry. They can provide valuable insights and may even refer you to opportunities within Medpace.
✨Tip Number 3
Prepare to discuss how your PhD research can be applied to clinical project management. Think about specific examples where you've demonstrated analytical skills or project coordination that align with the responsibilities of an Associate Clinical Trial Manager.
✨Tip Number 4
Showcase your adaptability and eagerness to learn during any interactions with Medpace. Highlighting your willingness to undergo intensive training and grow within the company can set you apart from other candidates.
We think you need these skills to ace Associate Clinical Trial Manager (PhD) - Renal
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your PhD in Life Sciences and any relevant research experience. Emphasise skills that align with the responsibilities of the Associate Clinical Trial Manager role, such as project management and collaboration.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical trial management and your desire to apply your analytical skills in a practical setting. Mention specific experiences from your PhD that demonstrate your ability to manage projects and work in a team.
Highlight Relevant Skills: In your application, focus on skills that are crucial for the role, such as communication, attention to detail, and the ability to work in a fast-paced environment. Provide examples of how you've demonstrated these skills during your academic career.
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 and its relevance to clinical trials. Be ready to explain how your background makes you a great fit for Medpace.
How to prepare for a job interview at Medpace
✨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 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.
✨Familiarise Yourself with Clinical Trial Processes
Even if you lack direct experience in the CRO or pharmaceutical industry, showing a basic understanding of clinical trial phases and management processes can set you apart. Research common terminologies and practices in the field.
✨Express Your Desire for Growth
Medpace values candidates who are eager to learn and grow. Be ready to discuss your career aspirations and how you see yourself progressing within the company, especially in relation to the accelerated career path they offer.
