Senior Clinical Research Project Coordinator - Denver
Medpace, Inc.·Denver, Colorado
Medpace, Inc.·Denver, Colorado
The role involves engaging in day-to-day clinical trial management, working closely with the CTM to ensure timely and accurate task delivery. Responsibilities also include compiling status reports, interacting with various stakeholders, and managing internal regulatory filing oversight and study supplies.
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.
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.
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 6,000 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.
Candidates must possess a Bachelor's degree in a health or life sciences field and should have prior experience as a Study Coordinator or within the pharmaceutical industry. Excellent skills in computer applications, organization, and communication are also required.
Market context
In Colorado, administration roles in clinical research often draw steady interest because employers look for candidates who can coordinate studies, manage documentation, and support compliance. This role is competitive because it asks for a bachelor’s degree, clinical research experience, and preferred skills in science-related study, electronic data capture systems, and project management. Review the AI-summarized requirements and benefits here to save time, then tailor your application to show direct research coordination experience.
