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- Tasks: Join our Clinical Trial Management team to oversee and manage clinical trial activities.
- Company: Medpace is a leading clinical contract research organization dedicated to advancing medical therapeutics.
- Benefits: Enjoy flexible work, competitive pay, PTO, and career growth opportunities.
- Why this job: Make a real impact in healthcare while developing your career in a dynamic international environment.
- Qualifications: PhD in Life Sciences required; no prior industry experience needed but is a plus.
- Other info: Intensive training provided for recent PhD graduates looking to excel in Clinical Trial Management.
The predicted salary is between 36000 - 60000 £ per year.
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.
Want to make an application Make sure your CV is up to date, then read the following job specs carefully before applying.
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.
EO/AA Employer M/F/Disability/Vets
Associate Clinical Trial Manager (PhD) - Oncology employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Trial Manager (PhD) - Oncology
✨Tip Number 1
Familiarize yourself with the clinical trial management process. Understanding the key components of clinical trials, including regulatory requirements and project timelines, will help you stand out as a candidate who is ready to hit the ground running.
✨Tip Number 2
Network with professionals in the clinical research field. Attend industry conferences or webinars to connect with current Clinical Trial Managers or Project Coordinators. This can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Highlight your analytical skills during interviews. Since the role requires applying academic skills in project management, be prepared to discuss specific examples from your PhD or post-doctoral research that demonstrate your ability to analyze data and manage projects effectively.
✨Tip Number 4
Show enthusiasm for the oncology field. Research recent advancements in oncology therapeutics and be ready to discuss how your background aligns with Medpace's mission. This will demonstrate your genuine interest in contributing to their impactful work.
We think you need these skills to ace Associate Clinical Trial Manager (PhD) - Oncology
Some tips for your application 🫡
Highlight Your PhD Experience: Make sure to emphasize your PhD and any post-doctoral research experience in your application. Detail how your academic background has prepared you for the role of Associate Clinical Trial Manager, particularly in oncology.
Showcase Analytical Skills: Demonstrate your analytical skills in your CV and cover letter. Provide examples of how you've applied these skills in previous research or projects, especially in a clinical or project management context.
Tailor Your Application: Customize your application materials to reflect the specific responsibilities and qualifications mentioned in the job description. Use keywords from the listing to align your experience with what Medpace is looking for.
Express Your Desire for Growth: In your cover letter, express your enthusiasm for the opportunity to grow within the clinical trial management field. Mention your willingness to undergo intensive training and your ambition for an accelerated career path.
How to prepare for a job interview at Medpace
✨Showcase Your Analytical Skills
As an Associate Clinical Trial Manager, you'll need to apply your analytical skills effectively. Be prepared to discuss specific examples from your PhD or post-doctoral research where you utilized these skills in project management or data analysis.
✨Demonstrate Team Collaboration
Highlight your experience working in teams, especially in international settings. Medpace values collaboration, so share instances where you successfully communicated and collaborated with diverse groups to achieve project goals.
✨Prepare for Fast-Paced Environments
The clinical trial management field is dynamic and fast-paced. Discuss how you've adapted to changing circumstances in your previous roles or research projects, showcasing your ability to thrive under pressure.
✨Understand the Role of aCTM
Familiarize yourself with the responsibilities of an Associate Clinical Trial Manager. Be ready to explain how your background aligns with tasks like maintaining project timelines, overseeing regulatory filings, and managing study supplies.
