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- 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 patients' 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.
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 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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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
Familiarise yourself with the clinical trial management process. Understanding the key stages and responsibilities involved will help you speak confidently about how your academic background can translate into practical skills during interviews.
✨Tip Number 2
Network with professionals in the clinical research field. Attend relevant conferences or webinars, and connect with people on platforms like LinkedIn. This can provide insights into the industry and may even lead to referrals for positions at Medpace.
✨Tip Number 3
Prepare to discuss your analytical skills and how they apply to project management. Be ready to give examples from your PhD or post-doctoral research that demonstrate your ability to manage complex data and collaborate with diverse teams.
✨Tip Number 4
Show enthusiasm for the role and the company’s mission. Research Medpace’s recent projects and achievements in the clinical trial space, and be prepared to articulate why you want to contribute to their goals during your interview.
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 research and your desire to transition into the industry. Mention specific experiences from your academic background that demonstrate your readiness for the role.
Highlight Relevant Skills: In your application, focus on skills that are crucial for the Associate Clinical Trial Manager position, such as communication, collaboration, and attention to detail. Provide examples of how you've used these skills in your previous work or research.
Proofread Your Application: Before submitting, thoroughly proofread your application materials. Check for grammatical errors and ensure that all information is clear and concise. A polished application reflects your professionalism and attention to detail.
How to prepare for a job interview at Medpace
✨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 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 you can thrive in Medpace's international team.
✨Prepare for Technical Questions
Expect questions related to clinical trial processes and regulatory requirements. Brush up on your knowledge of these areas, as it will demonstrate your readiness to transition into the industry.
✨Express Your Career Aspirations
Medpace values candidates who are eager to grow. Clearly articulate your career goals and how this position aligns with your aspirations in clinical trial management, showing your commitment to an accelerated career path.
