At a Glance
- 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.
- Other info: Intensive training provided; no prior experience in CRO or pharma needed.
- 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.
The predicted salary is between 30000 - 40000 € per year.
Medpace is currently seeking candidates with 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. Candidate 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 6,000 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) in London employer: Medpace, Inc.
Medpace is an exceptional employer for those looking to transition from a junior doctor role into the dynamic field of clinical research. With a strong commitment to employee development, we offer comprehensive training, a flexible work environment, and structured career paths that empower our team members to grow professionally while making a meaningful impact on global health. Located in London, our collaborative culture fosters innovation and teamwork, ensuring that every employee feels valued and engaged in their work.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Clinical Trial Manager - (Junior Doctor Background) in London
✨Network Like a Pro
Get out there and connect with people in the clinical research field! Attend industry events, join relevant online forums, and don’t be shy about reaching out to professionals on LinkedIn. We all know that sometimes it’s not just what you know, but who you know!
✨Ace the Interview
Prepare for your interviews by researching Medpace and understanding their mission and values. Practice common interview questions and think about how your background as a junior doctor can bring value to the Associate Clinical Trial Manager role. We want to see your passion and how you can contribute!
✨Showcase Your Skills
During interviews or networking, highlight your analytical and academic skills. Share examples of how you've applied these in your medical training. We love to see candidates who can demonstrate their ability to adapt and thrive in a fast-paced environment!
✨Apply Through Our Website
Don’t forget to apply directly through the Medpace website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows your enthusiasm for joining our team. Let’s get you started on this exciting career path together!
We think you need these skills to ace Associate Clinical Trial Manager - (Junior Doctor Background) in London
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. Be genuine and let your personality come through.
Showcase Your Communication Skills:Since this role involves a lot of collaboration, emphasise your communication skills in your application. Mention any experiences where you've successfully worked in teams 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 super easy, and you’ll be able to keep track of your application status!
How to prepare for a job interview at Medpace, Inc.
✨Know Your Stuff
Make sure you brush up on your clinical knowledge and the basics of clinical trial management. Familiarise yourself with common terminologies and processes in the industry, 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 points.
✨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. Ask about the training process, team dynamics, or how success is measured in the role.
✨Be Yourself
While professionalism is key, don’t forget to let your personality shine through. Medpace values passion and purpose, so share what drives you and why you want to make a difference in clinical research. Authenticity can set you apart from other candidates.
