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For Companies At a Glance
- Tasks: Join our team to manage clinical trials and collaborate on global study activities.
- Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics.
- Benefits: Enjoy flexible work, competitive pay, professional growth opportunities, and wellness initiatives.
- Why this job: Kickstart your career in a dynamic environment while making a real impact on patient lives.
- Qualifications: PhD in Life Sciences required; no prior industry experience needed but is a plus.
- Other info: Intensive training provided for recent graduates aiming for rapid career advancement.
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 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.
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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
Network with professionals in the clinical trial management field, especially those who have experience in oncology. Attend industry conferences or webinars to connect with potential colleagues and learn more about the role.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical trials, particularly in oncology. This knowledge will not only boost your confidence but also demonstrate your commitment to the field during interviews.
✨Tip Number 3
Prepare to discuss how your PhD research can be applied to clinical trial management. Think of specific examples where your analytical skills and project management experience can contribute to the success of clinical studies.
✨Tip Number 4
Showcase your ability to work in a team by highlighting any collaborative projects from your academic background. Emphasising your teamwork skills will align well with the collaborative nature of the Associate Clinical Trial Manager role.
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 from your academic background that demonstrate your readiness for the role.
Highlight Relevant Skills: In your application, focus on skills like communication, collaboration, and attention to detail. These are crucial for the Associate Clinical Trial Manager position and should be evident in your examples.
Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no typos or grammatical errors, 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 an Associate Clinical Trial Manager, you'll need to demonstrate your ability to apply analytical skills in project management. Be prepared to discuss specific examples from your PhD or post-doctoral research where you successfully analysed data or solved complex problems.
✨Understand the Clinical Trial Process
Familiarise yourself with the clinical trial process and the role of a Clinical Trial Manager. Research Medpace's approach to clinical trials, especially in oncology, and be ready to discuss how your background aligns with their mission and values.
✨Prepare for Team Collaboration Questions
Since the role involves working closely with project coordinators and other team members, expect questions about teamwork and collaboration. Think of instances where you effectively communicated and collaborated on projects during your academic career.
✨Demonstrate Your Passion for the Industry
Medpace is looking for candidates who are passionate about making a difference in the field of therapeutics. Be sure to express your enthusiasm for clinical research and how your experiences have prepared you for this role in a dynamic environment.
