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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 with solid training and impactful projects.
- Qualifications: PhD in Life Sciences and strong English presentation skills required; prior industry experience is a plus.
- Other info: Recognised by Forbes as one of America's Most Successful Midsize Companies.
The predicted salary is between 28800 - 48000 £ 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. 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.
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
- Manage and perform 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) - Neuroscience / Ophthalmology employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology
✨Tip Number 1
Network with professionals in the clinical trial management field, especially those who have experience in neuroscience or ophthalmology. Attend relevant conferences or webinars to meet potential colleagues and learn more about the industry.
✨Tip Number 2
Familiarise yourself with clinical trial management systems and tools that are commonly used in the industry. This knowledge will not only boost your confidence but also demonstrate your proactive approach to learning.
✨Tip Number 3
Prepare to discuss your PhD research in a way that highlights its relevance to clinical trials. Be ready to explain how your analytical skills can be applied to project management and problem-solving in a clinical setting.
✨Tip Number 4
Show enthusiasm for the role and the company during any interactions. Research Medpace’s recent projects and achievements, and be prepared to discuss how you can contribute to their mission of developing safe and effective medical therapeutics.
We think you need these skills to ace Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your PhD and any relevant research experience, especially in neuroscience or ophthalmology. 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 clinical trial management and your desire to transition from academia to industry. Mention specific experiences that demonstrate your ability to work in a team and manage projects effectively.
Highlight Relevant Skills: In your application, focus on skills that are crucial for the role, such as communication, collaboration, and attention to detail. Provide examples of how you've used these skills in your academic or research work.
Prepare for Potential Questions: Anticipate questions related to your research background and how it applies to clinical trials. Be ready to discuss your understanding of the clinical trial process and your motivation for joining Medpace.
How to prepare for a job interview at Medpace
✨Showcase Your Research Skills
As a PhD holder, you have a wealth of research experience. Be prepared to discuss your previous projects in detail, highlighting how your analytical skills can be applied to clinical trial management.
✨Demonstrate Team Collaboration
The role involves working closely with various teams. Share examples of how you've successfully collaborated in the past, especially in dynamic environments, to show that you're a team player.
✨Prepare for Technical Questions
Expect questions related to clinical trial processes and regulations. Brush up on your knowledge of the industry and be ready to discuss how your academic background aligns with the responsibilities of the role.
✨Express Your Career Aspirations
Medpace values candidates who are eager to grow. Clearly articulate your career goals and how this position fits into your long-term plans, demonstrating your commitment to the field.
