Find a job 
Featured Companies 
Featured Universities 
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 focused on advancing therapeutics.
- Benefits: Enjoy foundational training, an international work environment, and career development opportunities.
- Why this job: Perfect for recent PhD graduates eager to apply their skills in a dynamic industry.
- Qualifications: PhD in Life Sciences and strong English presentation skills required.
- Other info: No prior experience in CRO or pharmaceutical industry needed, but it's a plus.
The predicted salary is between 36000 - 60000 £ per year.
Medpace is currently seeking candidates with Cardiovascular related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London 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 (RO). 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.
#J-18808-Ljbffr
Associate Clinical Trial Manager (PhD) - Cardiovascular employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Trial Manager (PhD) - Cardiovascular
✨Tip Number 1
Network with professionals in the clinical trial management field, especially those who have transitioned from academia to industry. Attend relevant conferences or webinars to meet potential colleagues and learn about their experiences.
✨Tip Number 2
Familiarise yourself with the latest trends and technologies in clinical trial management. This knowledge will not only help you during interviews but also demonstrate your commitment to staying current in the field.
✨Tip Number 3
Consider reaching out to current or former employees at Medpace through platforms like LinkedIn. Ask them about their experiences and any advice they might have for someone looking to join the team.
✨Tip Number 4
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 add value to the role.
We think you need these skills to ace Associate Clinical Trial Manager (PhD) - Cardiovascular
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your PhD in Life Sciences 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: In your cover letter, express your enthusiasm for the role and the company. Discuss how your academic background and skills make you a great fit for the Associate Clinical Trial Manager position, and mention your desire to grow within the industry.
Highlight Relevant Skills: Focus on skills that are crucial for the role, such as communication, collaboration, and attention to detail. Provide examples from your academic or research experiences that demonstrate these abilities.
Proofread Your Application: Before submitting, carefully 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 Academic Background
As a candidate with a PhD in Life Sciences, make sure to highlight your research experience and how it relates to clinical trial management. Be prepared to discuss specific projects you've worked on and the analytical skills you've developed.
✨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, whether in presentations or team discussions.
✨Familiarise Yourself with Clinical Trial Processes
Even if you haven't worked directly in a CRO or pharmaceutical setting, understanding the basics of clinical trial management will give you an edge. Research common terminologies and processes to show your enthusiasm for the field.
✨Express Your Desire for Growth
The position offers an accelerated career path, so convey your eagerness to learn and develop within the role. Discuss your long-term career goals and how this position aligns with them, demonstrating your commitment to the industry.
