Associate Clinical Trial Manager – Oncology / Radiopharmaceuticals / Renal / Cardiovascular

Job title:

Associate Clinical Trial Manager – Oncology / Radiopharmaceuticals / Renal / Cardiovascular

Company

Medpace

Job description

Job Summary :Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging / radiopharmaceuticals or / radiation oncology for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work 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 radiopharmaceuticals (molecular radiotherapy, radiotheranostics, targeted radionuclide therapy). 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 Radiopharmaceuticals (nuclear medicine/medical physics/medical imaging/radiation oncology or related)
  • 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 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 NextA 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

Expected salary

Location

Stirling

Job date

Thu, 01 May 2025 04:03:56 GMT

To help us track our recruitment effort, please indicate in your email/cover letter where (globalvacancies.org) you saw this job posting.

yonnetim

Share
Published by
yonnetim

Recent Posts

Senior Specialist for Stakeholder Engagement, Governance and Gender

Procurement Process IC - Individual contractor Office UNDP-IDN - INDONESIA Deadline 17-Jul-26 @ 06:00 AM…

1 hour ago

IC 00832-2026 Expert on tax issues – automatic exchange of information for tax

Procurement Process IC - Individual contractor Office UNDP-MKD - Republic of North Macedonia Deadline 17-Jul-26…

1 hour ago

View Vacancy – JOA – Chevening and Political Support Officer (AO)

JOA - Chevening and Political Support Officer (AO) To apply please copy and paste this…

1 hour ago

LBN/CO/RFP/143/26 Assessment And Mapping Ciivil Defense

Procurement Process RFP - Request for proposal Office UNDP-LBN - LEBANON Deadline 23-Jul-26 @ 08:00…

1 hour ago

Consultant to review of the National Disability Policy (NDP, 2021)

Procurement Process IC - Individual contractor Office UNDP-ZWE - ZIMBABWE Deadline 13-Jul-26 @ 06:50 AM…

1 hour ago

LBN-CO-RFQ-141-26 Solar Photovoltaic (PV) Systems at the Lebanese Parliament

Procurement Process RFQ - Request for quotation Office UNDP-LBN - LEBANON Deadline 17-Jul-26 @ 08:00…

1 hour ago
If you dont see Apply Link. Please use non-Amp version