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- Tasks: Join our team as an Associate Clinical Trial Manager, managing clinical trial activities and collaborating with global teams.
- Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics worldwide.
- Benefits: Enjoy hybrid work options, competitive PTO, wellness initiatives, and structured career growth opportunities.
- Why this job: This role offers a unique chance to transition from academia to impactful clinical research in a dynamic environment.
- Qualifications: PhD in Life Sciences required; experience in oncology or related fields is a plus.
- Other info: Event on 8th May 2025 in Central London; apply by 5th May 2025.
The predicted salary is between 36000 - 60000 £ per year.
Medpace is delighted to host a Recruitment Event tailored to candidates studying or holding a PhD in Life Science. This is a rare and exciting opportunity for individuals seeking to make a switch from academia to the Clinical Trials Industry!
LOCATION: Central London
DATE: 8th of May 2025
APPLICATION CLOSE DATE: 5th of May 2025
At this event, Medpace is seeking to meet candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) role to join our global Clinical Operations team. The aCTM will be working closely with Project Coordinators and Clinical Trial Managers in 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.
This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and accelerate 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
- A background in one of our key therapeutic focus areas is of advantage, but not a must: Oncology, Cardiovascular, Renal / Gastrointestinal, Nuclear Medicine, or Radiopharmaceuticals
- Fluency in English with solid presentation skills
- Ability to work in a fast-paced dynamic industry within an international team
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?
- Hybrid work-from-home options (dependent upon position and level)
- Competitive PTO packages
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Flexible work schedule
- Competitive compensation and benefits package
- Structured career paths with opportunities for professional growth
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
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
PhD Career Event: Clinical Trial Management - Medpace London employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land PhD Career Event: Clinical Trial Management - Medpace London
✨Tip Number 1
Make sure to research Medpace thoroughly before the event. Understand their mission, values, and recent projects in clinical trial management. This knowledge will help you engage in meaningful conversations and demonstrate your genuine interest in the company.
✨Tip Number 2
Prepare specific questions related to the Associate Clinical Trial Manager role and the clinical trials industry. Asking insightful questions not only shows your enthusiasm but also helps you assess if this is the right fit for you.
✨Tip Number 3
Network with other attendees and Medpace representatives during the event. Building connections can provide valuable insights into the company culture and may even lead to referrals or recommendations for the position.
✨Tip Number 4
Follow up after the event with a thank-you email to the recruiters you spoke with. Express your appreciation for their time and reiterate your interest in the Associate Clinical Trial Manager role. This small gesture can leave a lasting impression.
We think you need these skills to ace PhD Career Event: Clinical Trial Management - Medpace London
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the Associate Clinical Trial Manager role. Review the job description carefully and note the key responsibilities and qualifications required.
Tailor Your CV: Customise your CV to highlight relevant experience and skills that align with the clinical trial management field. Emphasise your PhD research and any transferable skills that would be beneficial in this role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for transitioning from academia to the clinical trials industry. Mention specific experiences that demonstrate your analytical skills and ability to work in a team.
Prepare for the Event: Since this is a recruitment event, prepare to discuss your background and how it relates to the role. Be ready to ask insightful questions about Medpace and the clinical trial management process.
How to prepare for a job interview at Medpace
✨Research Medpace and the Role
Before the interview, take some time to research Medpace and understand their mission, values, and recent projects. Familiarise yourself with the Associate Clinical Trial Manager role and how your PhD skills can be applied in this context.
✨Prepare for Behavioural Questions
Expect questions that assess your problem-solving abilities and teamwork skills. Prepare examples from your academic experience that demonstrate your analytical skills, ability to work under pressure, and collaboration with others.
✨Show Enthusiasm for Transitioning to Industry
Express your excitement about moving from academia to the clinical trials industry. Highlight your desire to apply your research skills in a practical setting and your commitment to contributing to the development of therapeutics.
✨Ask Insightful Questions
Prepare thoughtful questions to ask the interviewers about the company culture, training opportunities, and career progression within Medpace. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
