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- Tasks: Join our team to manage clinical trials and collaborate globally.
- Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics.
- Benefits: Enjoy flexible work, competitive pay, and structured career growth opportunities.
- Why this job: Make a real impact in healthcare while developing your career in a dynamic environment.
- Qualifications: PhD in Life Sciences required; no prior industry experience needed but beneficial.
- Other info: Intensive training provided for recent graduates looking to excel in Clinical Trial Management.
The predicted salary is between 28800 - 48000 £ per year.
Overview Medpace is currently seeking candidates with Oncology 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. 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 OverviewMedpace 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 NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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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
Network with professionals in the clinical trial management field, especially those who have transitioned from academia to industry. Attend relevant conferences or webinars where you can meet people from Medpace or similar organisations.
✨Tip Number 2
Familiarise yourself with the latest trends and technologies in clinical trial management. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in a fast-paced industry.
✨Tip Number 3
Prepare to discuss how your PhD research can be applied to clinical project administration. Think about specific examples where your analytical skills can contribute to managing clinical trials effectively.
✨Tip Number 4
Showcase your ability to work in international teams by highlighting any collaborative projects you've been involved in during your studies. This will align well with Medpace's global focus and team dynamics.
We think you need these skills to ace Associate Clinical Trial Manager (PhD) - Oncology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your PhD and any relevant research experience. Emphasise skills that align with clinical trial management, such as analytical abilities and project coordination.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for oncology and clinical trials. Mention specific experiences that demonstrate your ability to work in a fast-paced environment and your desire to grow within the industry.
Highlight Relevant Skills: In your application, focus on skills like communication, collaboration, and attention to detail. These are crucial for the role of Associate Clinical Trial Manager and should be evident in your examples.
Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no grammatical errors or typos, as these can detract from your professionalism and attention to detail.
How to prepare for a job interview at Medpace
✨Showcase Your Analytical Skills
As a candidate with a PhD, it's crucial to highlight your analytical and academic skills during the interview. Be prepared to discuss specific examples from your research that demonstrate your ability to analyse data and solve complex problems, as these skills are essential for the Associate Clinical Trial Manager role.
✨Familiarise Yourself with Clinical Trials
Even if you don't have prior experience in the CRO or pharmaceutical industry, showing a solid understanding of clinical trial processes can set you apart. Research the phases of clinical trials, key terminology, and current trends in oncology to demonstrate your enthusiasm and readiness to learn.
✨Prepare for Team Collaboration Questions
Since the role involves working closely with project coordinators and clinical trial managers, be ready to answer questions about teamwork and collaboration. Think of examples where you've successfully worked in a team setting, especially in a fast-paced environment, and how you contributed to achieving common goals.
✨Practice Your Presentation Skills
Fluency in English and strong presentation skills are vital for this position. Prepare to articulate your thoughts clearly and confidently. You might even want to practice presenting your research findings or discussing a relevant topic to ensure you're comfortable speaking in front of others during the interview.
