Clinical Trial Project Manager - Denver, CO

Medpace, Inc. • Denver, CO

115d • Onsite

About The Position

Medpace is hiring a Clinical Trial Project Manager to join its Clinical Trial Management Group in Denver, Colorado. The role manages clinical study operations in accordance with the contract, ICH/GCP, and applicable laws and regulations. The Project Manager serves as the primary operational contact for the Sponsor, provides cross-functional oversight of the internal project team, manages study risks and vendors, and oversees site quality and clinical research associates. Medpace conducts clinical development across therapeutic areas including oncology/hematology, cardiovascular/metabolic disease, infectious disease, and neuroscience.

Medpace is a full-service clinical contract research organization providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. The company is headquartered in Cincinnati, Ohio, and employs more than 6,500 people across 40+ countries. This is an office-based role, with occasional work-from-home flexibility for eligible positions after training.

The target salary range is $100,000–$190,000, with potential for bonus and equity awards. Compensation is based on skills and experience. Benefits for full-time positions include medical, dental, and vision coverage; 401(k); vacation, sick days, and paid holidays; work-from-home flexibility; short- and long-term disability; health savings and flexible spending accounts; life and AD&D insurance; pet insurance; and reimbursement for travel expenses. Medpace also describes employee development programs, company-sponsored social events, and comprehensive health, wellness, retirement, and PTO benefits. Benefits may vary by country.

Requirements

• Bachelor’s degree in a health-related field.
• Experience in clinical trials across Phases 1–4.
• Two to five years of experience as a project manager or clinical trial manager.
• Experience managing the overall project timeline.
• Strong leadership skills.

Nice To Haves

• Advanced degree in a health-related field.
• Experience in Phases 2–3 is preferred.

Responsibilities

• Manage and ensure accountability for day-to-day project operations according to the contract, ICH/GCP, and applicable laws, rules, and regulations.
• Serve as the primary Sponsor contact for operational project-specific issues and study deliverables.
• Maintain in-depth knowledge of the protocol, therapeutic area, and indication.
• Provide cross-functional oversight of internal project team members and deliverables, including ensuring project-specific training is provided.
• Review and provide input on the study protocol, edit check specifications, data analysis plan, and final study report, when applicable.
• Develop operational project plans.
• Manage risk assessment and execution.
• Manage study vendors.
• Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.

Benefits

• Competitive salary and bonus program, with potential for bonus and equity awards.
• 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 spending accounts.
• Life and AD&D insurance.
• Pet insurance.
• Reimbursement for travel expenses, including food and gas allowance, rental cars, and hotel accommodations.
• Comprehensive health, wellness, retirement, and PTO benefits.
• Company-sponsored social events.
• On-site mentors, defined career paths, onboarding and training programs, and ongoing learning and development opportunities.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level