• Job Description

  Req#: 10654
  Job Summary
  
  
  Medpace is a leading CRO for Biotech companies and we are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology and more. If you are looking for a fast paced, collaborative work environment in clinical research and want to develop your career even further, then this is the opportunity for you. Medpace provides Project Coordinators a 4-6 week training program that incorporates a virtual and hands on learning experience, especially for those without previous clinical research experience.
  
  Responsibilities
  
  
  • Engage in clinical trial management on a day to day level;
  • Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy;
  • Compile and maintain project-specific status reports;
  • Interact with the Sponsor, study sites, and internal associates;
  • Provide oversight and quality control of our internal regulatory filing system;
  • Manage study supplies;
  • Create and maintain project timelines; and
  • Coordinate project meetings and produce quality meeting minutes.
  
  Qualifications
  
  
  • Bachelor's degree in a health/life sciences field;
  • Prior experience as a Study Coordinator or within the pharmaceutical industry; and
  • Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.
  Compensation
  A target salary range of $40,000 - $85,000. Your compensation will be based on your skills and experience. Medpace offers the following benefits for eligible positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, and pet insurance. For more details, please discuss with your recruiter.
  
  Medpace Overview
  
  
  Medpace is a full-service clinical contract research organization (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.
  Denver Perks
  • Denver Office Overview
  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Structured career paths with opportunities for professional growth
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • RTD Eco Pass
  • Secure bike storage room
  Awards
  • Named a Top Workplace in 2024 by The Cincinnati Enquirer

  • 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.
  
  
  • Bachelor's degree in a health/life sciences field;
  • Prior experience as a Study Coordinator or within the pharmaceutical industry; and
  • Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.
  Compensation
  A target salary range of $40,000 - $85,000. Your compensation will be based on your skills and experience. Medpace offers the following benefits for eligible positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, and pet insurance. For more details, please discuss with your recruiter.
  
  
  • Engage in clinical trial management on a day to day level;
  • Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy;
  • Compile and maintain project-specific status reports;
  • Interact with the Sponsor, study sites, and internal associates;
  • Provide oversight and quality control of our internal regulatory filing system;
  • Manage study supplies;
  • Create and maintain project timelines; and
  • Coordinate project meetings and produce quality meeting minutes.

• About the company

  Medpace Holdings, Inc. is a midsize, clinical contract research organization based in Cincinnati, Ohio.

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