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- Tasks: Join our Clinical Trial Management team to oversee and manage clinical trial activities.
- Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics globally.
- Benefits: Enjoy flexible work, competitive pay, professional growth opportunities, and wellness initiatives.
- Why this job: Kickstart your career with intensive training in a dynamic, international environment making a real impact.
- 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 for four consecutive years.
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. 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.
- 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.
Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology employer: Medpace, Inc.
Contact Detail:
Medpace, Inc. 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 the latest trends and technologies in clinical trial management. This will not only enhance your understanding but also demonstrate your commitment to staying current in the field during interviews.
✨Tip Number 3
Prepare to discuss how your PhD research can be applied to clinical project administration. Think of specific examples where your analytical skills can contribute to managing clinical trials effectively.
✨Tip Number 4
Show enthusiasm for the role and the company during any interactions. Research Medpace’s mission and values, and be ready to explain why you want to be part of their team and how you align with their goals.
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. 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 neuroscience or ophthalmology. Explain why you want to transition into clinical trial management and how your academic background prepares you for this role.
Highlight Relevant Skills: In your application, focus on skills like communication, collaboration, and attention to detail. Mention any experience with project management or teamwork, even if it's from academic projects.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is clear and concise to make a strong impression.
How to prepare for a job interview at Medpace, Inc.
✨Showcase Your Research Skills
As a PhD candidate, your research skills are invaluable. Be prepared to discuss your previous research projects in detail, highlighting how they relate to clinical trial management and the specific therapeutic areas Medpace focuses on.
✨Demonstrate Team Collaboration
The role involves working closely with various teams. Share examples of how you've successfully collaborated in past projects, especially in dynamic environments, to show that you can thrive in a team-oriented setting.
✨Prepare for Technical Questions
Expect questions related to clinical trial processes and regulatory requirements. Brush up on your knowledge of these areas, as well as any relevant software tools, to demonstrate your readiness for the role.
✨Express Your Career Aspirations
Medpace is looking for candidates eager to grow within the company. Clearly articulate your career goals and how this position aligns with your aspirations in clinical trial management, showing your commitment to long-term development.
