At a Glance
- Tasks: Manage clinical trials and collaborate with global teams to ensure project success.
- Company: Join Medpace, a leading clinical research organisation dedicated to advancing medical therapeutics.
- Benefits: Enjoy competitive pay, health benefits, and flexible work options after training.
- Other info: Dynamic environment with clear career paths and ongoing professional development.
- Why this job: Kickstart your career in clinical research with hands-on training and real-world impact.
- Qualifications: PhD or Post-Doc in Endocrinology/Metabolic; strong communication skills required.
The predicted salary is between 29700 - 36300 £ per year.
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in Endocrinology / Metabolic related areas for the office-based Associate Clinical Trial Manager (aCTM) position to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in the 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 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 or Post-Doc related to Endocrinology and/or Metabolic research.
- 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.
Other Employee Benefits:
- Competitive compensation programs that recognize and reward performance.
- Comprehensive health, wellness, retirement, and PTO benefits.
- Office-based culture with occasional WFH that provides flexibility for eligible positions after training.
- Company-sponsored social events.
Please note benefits may vary based on country.
What to Expect Next: A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Associate Clinical Trial Manager - Metabolic / Endocrinology in City of London employer: Medpace, Inc.
Medpace, Inc. is an excellent employer for those looking to kickstart their career in clinical trials, offering comprehensive onboarding and training that empowers you to become a data monitoring expert. With a strong emphasis on cross-functional collaboration and a supportive work culture, employees are encouraged to grow and develop their skills in a dynamic environment. Located in a vibrant office setting, Medpace provides a unique opportunity to contribute meaningfully to impactful projects while enjoying a fulfilling work-life balance.
