Senior Clinical Research Project Coordinator - Denver

Medpace; Denver (CO); On-site; USD 40,000 - 85,000; Full time

Job summary

A leading CRO for Biotech is seeking a full-time Project Coordinator to join their Clinical Trial Management team in Denver. This role offers a comprehensive training program and involves managing clinical trials, ensuring accuracy, and interacting with various stakeholders. Ideal candidates will have a Bachelor's degree in health/life sciences and strong organizational skills, with competitive compensation and benefits.

Benefits

Flexible work environment

Competitive PTO packages starting at 20+ days

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Discounts on local sports games and fitness gyms

Modern eco-friendly campus with fitness center

Structured career paths for professional growth

Qualifications

• Bachelor's degree in health/life sciences required.
• Prior experience as a Study Coordinator or similar role preferred.
• Excellent communication and organizational skills needed.

Responsibilities

• Engage in daily clinical trial management tasks.
• Manage study supplies and create project timelines.
• Coordinate meetings and ensure accurate status reports.

Skills

Organizational skills

Communication skills

Excellent computer skills

Education

Bachelor's degree in health/life sciences

Tools

Word-processing

Databases

Excel

Windows

Job description

Job Summary

Medpace is a leading CRO for Biotech companies and we are currently seeking a full-time, office-basedProject Coordinatorto 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.