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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 an innovative field with impactful work and solid training.
- Qualifications: PhD or Post-Doc in relevant fields; no prior industry experience required but beneficial.
- Other info: Be part of a globally recognised company making a difference in patients' lives.
The predicted salary is between 36000 - 60000 £ per year.
Job Summary
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging/radiopharmaceuticals, or radiation oncology for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in the 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 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 radiopharmaceuticals (molecular radiotherapy, radiotheranostics, targeted radionuclide therapy). 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 or Post-Doc related to Radiopharmaceuticals (nuclear medicine/medical physics/medical imaging/radiation oncology or related)
- 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 organisation (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
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Associate Clinical Trial Manager - Radiopharmaceuticals employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Trial Manager - Radiopharmaceuticals
✨Tip Number 1
Network with professionals in the clinical trial management field, especially those who have experience in radiopharmaceuticals. Attend industry conferences or webinars to connect with potential colleagues and learn more about the latest trends and challenges in the sector.
✨Tip Number 2
Familiarise yourself with the clinical trial management systems commonly used in the industry. Being knowledgeable about these tools can give you an edge during interviews and demonstrate your readiness to hit the ground running.
✨Tip Number 3
Prepare to discuss your academic research and how it relates to clinical trial management. Highlight any relevant projects or experiences that showcase your analytical skills and ability to work in a team-oriented environment.
✨Tip Number 4
Showcase your passion for the field by staying updated on recent advancements in radiopharmaceuticals and clinical trials. This knowledge will not only help you in interviews but also demonstrate your commitment to contributing to the industry.
We think you need these skills to ace Associate Clinical Trial Manager - Radiopharmaceuticals
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your PhD or Post-Doctoral experience in relevant fields such as nuclear medicine or medical physics. Emphasise any research projects or skills that align with the responsibilities of an Associate Clinical Trial Manager.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical trial management and your desire to work in the radiopharmaceuticals field. Mention specific experiences that demonstrate your analytical skills and ability to collaborate in a team.
Highlight Relevant Skills: In your application, clearly outline your communication and organisational skills, as these are crucial for the role. Provide examples of how you've successfully managed projects or collaborated with teams in your academic or research settings.
Proofread Your Application: Before submitting, thoroughly proofread your application materials. Ensure there are no grammatical errors and that your documents are formatted professionally. A polished application reflects your attention to detail, which is vital in clinical trial management.
How to prepare for a job interview at Medpace
✨Showcase Your Academic Background
As a candidate with a PhD or Post-Doc, make sure to highlight your research experience in nuclear medicine or related fields. Discuss specific projects you've worked on and how they relate to the role of Associate Clinical Trial Manager.
✨Demonstrate Communication Skills
Since the role involves collaboration with various stakeholders, practice articulating your thoughts clearly. Prepare examples of how you've effectively communicated complex information in past experiences, especially in an international context.
✨Familiarise Yourself with Clinical Trial Processes
Even if you lack direct experience in the CRO or pharmaceutical industry, understanding the basics of clinical trial management will be beneficial. Research common practices and terminology to show your eagerness to learn and adapt.
✨Express Your Desire for Growth
Medpace values candidates who are keen on professional development. Be prepared to discuss your career aspirations and how you see yourself growing within the company, particularly in the field of radiopharmaceuticals.
