Job Title: Director of Clinical Trial Management
Location: Denver, Colorado
Department: Clinical Trial Management
Job ID: 10694
Employment Type: Full-time (Office-based with work-from-home flexibility after tenure)
Job Summary
Medpace is seeking an experienced Director of Clinical Trial Management to join our newly established Denver, CO office. This senior-level role is responsible for mentoring Clinical Trial Managers (CTMs), overseeing projects, managing sponsor relationships, and ensuring operational excellence across clinical trials in therapeutic areas including:
Oncology
Cardiovascular/Metabolic
Infectious Disease
Neuroscience
And more
The role offers a competitive salary, bonus program, and equity grants.
Key Responsibilities
Mentor Clinical Trial Managers, Project Coordinators, and other study team members.
Manage day-to-day operations of projects, ensuring compliance with ICH/GCP and applicable laws/regulations.
Serve as the primary Sponsor contact for operational and study deliverable issues.
Maintain in-depth knowledge of protocol, therapeutic area, and indication.
Provide cross-functional oversight of internal project team members, ensuring all project-specific training is completed.
Review and provide input for study protocols, edit check specifications, data analysis plans, and final study reports.
Develop operational project plans and manage risk assessment and execution.
Manage study vendors where applicable.
Oversee site quality and monitoring deliverables.
Collaborate with HR to support recruitment of new staff in the Denver office.
Act as an escalation point for Clinical Operations within the Denver office.
Implement and support Medpace corporate strategies locally.
Organize cross-functional leadership teams to align and support associates in the Denver office.
Qualifications
Bachelor’s degree in a health-related field (Advanced degree preferred).
Experience in Phases 1-4 clinical trials, with preference for Phases 2-3.
5+ years as a Project/Clinical Trial Manager within a CRO.
Experience managing overall project timelines.
Bid defense experience.
Strong leadership and mentorship skills.
Compensation & Benefits
Target Salary Range: $175,000 – $250,000 (based on experience)
Benefits Include:
Medical, dental, and vision insurance
401(k) plan
Paid vacation, sick days, and holidays
Work-from-home flexibility after tenure
Short-term and long-term disability coverage
Health savings and flexible savings accounts
Life and AD&D insurance
Pet insurance
About Medpace
Medpace is a full-service clinical CRO providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace has 5,000+ employees across 40+ countries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach.
Therapeutic expertise includes:
Oncology
Cardiology
Metabolic Disease
Endocrinology
Central Nervous System
Anti-viral & Anti-infective
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow.
Flexible work environment and modern, ecofriendly Denver campus
Competitive PTO starting at 20+ days
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Community involvement with local nonprofits
Structured career paths and professional growth opportunities
Discounts for local sports, gyms, and attractions
RTD Eco Pass and secure bike storage
Awards & Recognition
Named a Top Workplace in 2024 by The Cincinnati Enquirer
Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024)
CRO Leadership Awards from Life Science Leader magazine
Next Steps
A Medpace team member will review your qualifications and, if interested, contact you with details for next steps.
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