Senior Clinical Trials Project Lead

Medpace; Denver (CO); On-site; USD 75,000 - 110,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k)

Vacation policy

Sick days

Paid holidays

Work from home flexibility

Short-term disability

Long-term disability

Health savings and flexible savings

Life and AD&D insurance

Pet insurance

Travel expense reimbursement

Job summary

Medpace is a leading CRO delivering phase l-lV clinical development services. We are seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team and help drive successful study execution.

You will work with the CTM to support daily trial activities, prepare status reports, coordinate meetings, manage study supplies, and ensure timelines are met with high accuracy. This role includes a 4–6 week training program designed for rapid onboarding.

Qualifications

• Bachelor's degree in health/life sciences required.
• Experience as a Study Coordinator or in the pharmaceutical industry preferred.
• Strong computer skills including Word processing, databases, Excel, and Windows; excellent organizational and communication abilities.

Responsibilities

• Engage in clinical trial management on a day to day level.
• Work closely with the project CTM for timely delivery of tasks with high 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.
• Coordinate project meetings and produce meeting minutes.

Skills

Communication skills

Organizational skills

Project coordination

Education

Bachelor's degree in health/life sciences

Tools

Excel

Job description

Medpace is a leading CRO delivering phase l-lV clinical development services. We are seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team and help drive successful study execution.

You will work with the CTM to support daily trial activities, prepare status reports, coordinate meetings, manage study supplies, and ensure timelines are met with high accuracy. This role includes a 4–6 week training program designed for rapid onboarding.