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- Tasks: Join our team as an Associate Clinical Trial Manager, managing clinical trial activities.
- Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics.
- Benefits: Enjoy flexible work options, competitive pay, and structured career growth opportunities.
- Why this job: Make a real impact in healthcare while transitioning from academia to industry.
- Qualifications: PhD in Life Sciences required; experience in oncology or cardiology is a plus.
- Other info: Attend our recruitment event in Central London on 18th September 2024.
The predicted salary is between 28800 - 48000 £ 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: Thursday 18th September 2024
APPLICATION CLOSE DATE: Monday 14th September
Associate Clinical Trial Manager
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. Candidate 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).
What to Expect Next:
A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an RSVP.
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, Endocrine/metabolic, N uclear Medicine, or Radiopharmaceuticals
- Fluency in English with solid presentation skills
- Ability to work in a fast-paced dynamic industry within an international team
Medpace Overview
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?
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
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 transition from academia to industry. This shows your enthusiasm for the position and helps you gain insights into what the job entails, making you a more attractive candidate.
✨Tip Number 3
Network with other attendees and Medpace representatives during the event. Building connections can provide valuable insights and may lead to referrals or recommendations, increasing your chances of landing the job.
✨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 position. This keeps you on their radar and demonstrates your professionalism.
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 to identify key responsibilities and required qualifications.
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 aspirations clearly. Practice articulating how your academic experience can contribute to Medpace's mission and the role of an Associate Clinical Trial Manager.
How to prepare for a job interview at Medpace
✨Understand the Clinical Trial Landscape
Familiarise yourself with the basics of clinical trial management and the specific role of an Associate Clinical Trial Manager. Knowing key terms and processes will help you engage in meaningful discussions during the interview.
✨Highlight Your Transferable Skills
Emphasise how your PhD research and analytical skills can be applied to clinical project administration. Be ready to provide examples of how you've managed projects or collaborated with teams in your academic work.
✨Prepare for Behavioural Questions
Expect questions that assess your problem-solving abilities and teamwork. Use the STAR method (Situation, Task, Action, Result) to structure your responses and demonstrate your experience effectively.
✨Show Enthusiasm for the Industry
Express your passion for transitioning from academia to the clinical trials industry. Research Medpace's mission and values, and be prepared to discuss why you want to contribute to their goals in developing therapeutics.
