Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Manage clinical trials and collaborate with global teams to ensure project success.
- Company: Join Medpace, a leading clinical research organisation making a real impact in healthcare.
- Benefits: Enjoy flexible work, competitive pay, and structured career growth opportunities.
- Why this job: Kickstart your career in clinical trial management with hands-on training and international exposure.
- Qualifications: PhD in Life Sciences and strong communication skills required.
- Other info: Be part of a dynamic team dedicated to improving patient lives globally.
The predicted salary is between 30000 - 50000 £ per year.
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.
#J-18808-Ljbffr
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
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about introducing yourself. You never know who might have a lead on that perfect Associate Clinical Trial Manager role.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to clinical trial management. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your analytical skills during interviews! Be ready to discuss how your PhD research can translate into real-world applications in clinical project management. This is your chance to shine!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
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 is tailored to highlight your PhD and any relevant research experience. We want to see how your skills align with the role of Associate Clinical Trial Manager, so don’t hold back on showcasing your analytical abilities!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical trial management and how your background makes you a great fit for our team. Keep it engaging and personal – we love to see your personality come through.
Showcase Your Communication Skills: Since this role involves a lot of collaboration, make sure to highlight your communication skills in your application. Whether it’s through your CV or cover letter, let us know how you’ve effectively worked with teams in the past.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts and you’ll be set!
How to prepare for a job interview at Medpace
✨Know Your Stuff
Make sure you brush up on your PhD research and any relevant projects you've worked on. Be ready to discuss how your analytical skills can be applied in clinical trial management, especially in the renal field.
✨Show Your Team Spirit
Since you'll be working closely with project coordinators and clinical trial managers, highlight your collaboration skills. Share examples of how you've successfully worked in teams during your studies or previous roles.
✨Be Ready for Fast-Paced Questions
Medpace operates in a dynamic environment, so expect questions that assess your ability to handle pressure. Prepare scenarios where you managed tight deadlines or adapted quickly to changes in your research.
✨Ask Smart Questions
At the end of the interview, have some insightful questions ready about the role or the company culture. This shows your genuine interest and helps you gauge if Medpace is the right fit for you.