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- Tasks: Join our team to manage clinical trials and collaborate on global study activities.
- Company: Medpace, a leading clinical research organisation with a mission to improve lives.
- Benefits: Flexible work environment, competitive pay, and structured career growth opportunities.
- Why this job: Kickstart your career in clinical research and make a real difference in healthcare.
- Qualifications: Bachelor of Medicine, Bachelor of Surgery; strong communication skills required.
- Other info: Intensive training provided; no prior experience in CRO or pharma needed.
The predicted salary is between 30000 - 40000 £ per year.
Medpace is currently seeking candidates with a Bachelor of Medicine, Bachelor of Surgery qualification 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. Candidates must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
A fantastic opportunity for recent junior doctors to enter the clinical research industry in an operations role, 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
- Bachelor of Medicine, Bachelor of Surgery
- 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 - (Junior Doctor Background) employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Trial Manager - (Junior Doctor Background)
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. The more people you know, the better your chances of landing that aCTM role.
✨Tip Number 2
Prepare for interviews by brushing up on your clinical knowledge and project management skills. Practice common interview questions and think about how your junior doctor experience can translate into the aCTM role.
✨Tip Number 3
Show your enthusiasm for the role! During interviews, express your passion for clinical trials and your eagerness to learn. Employers love candidates who are genuinely excited about the work they'll be doing.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining the Medpace team.
We think you need these skills to ace Associate Clinical Trial Manager - (Junior Doctor Background)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Associate Clinical Trial Manager role. Highlight any relevant clinical experience or projects that showcase your analytical and academic skills.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for clinical research and how your background as a junior doctor makes you a great fit for the team. Keep it concise but impactful!
Showcase Your Communication Skills: Since the role involves collaboration with various teams, emphasise your communication skills in your application. Mention any experiences where you've successfully worked in a team or communicated complex information clearly.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s straightforward and ensures your application goes straight to the right people!
How to prepare for a job interview at Medpace
✨Know Your Stuff
Make sure you brush up on your medical knowledge and understand the basics of clinical trial management. Familiarise yourself with common terminologies and processes in clinical research, as this will show your enthusiasm and readiness to dive into the role.
✨Showcase Your Skills
Highlight your analytical and academic skills during the interview. Be prepared to discuss how your background as a junior doctor can translate into effective project administration and management. Use specific examples from your experience to illustrate your capabilities.
✨Ask Smart Questions
Prepare thoughtful questions about the role and the company. This not only shows your interest but also helps you gauge if Medpace is the right fit for you. Inquire about the training process, team dynamics, and opportunities for growth within the organisation.
✨Be Ready for Teamwork
Since the role involves collaboration with various teams, be ready to discuss your experiences working in a team environment. Share examples of how you've effectively communicated and collaborated with others, especially in high-pressure situations.