Clinical Trial Project Manager - Immunology - Denver

About the Role

Medpace is seeking established Clinical Trial Managers and Project Managers with a focus in Immunology, Rheumatology, Allergy, and/or Dermatology to join our Clinical Trial Management Group in our Denver, CO office.

Responsibilities

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

Requirements

• Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred.
• Experience in Phases 1-4; Phases 2-3 preferred.
• 3-5 years as a project/clinical trial manager within a CRO.
• Management of overall project timeline.
• Strong leadership skills.

Pay

A target salary range of $100,000 - $190,000 with potential for bonus and equity awards. Your compensation will be based on your skills and experience.

Benefits

• Medical, dental, vision insurance.
• 401(k) retirement plan.
• Vacation policy, sick days, and paid holidays.
• Work from home flexibility.
• Short-term and long-term disability insurance.
• Health savings and flexible savings accounts.
• Life and AD&D insurance.
• Pet insurance.
• Reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations).

About Medpace

Medpace is a full-service clinical contract research organization (CRO) providing 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

• Purpose-Driven Work: Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence.
• Collaborative Culture: Contribute to an interactive team environment that empowers decision-making, creative thinking, and continuous learning through open communication and mutual trust. Leadership is both accessible and approachable.
• Continuous Growth & Development:
  • Office-based environment with on-site mentors.
  • Defined career paths with clear advancement opportunities.
  • Industry-renowned onboarding and training programs designed to accelerate professional development.
  • Ongoing training and continuous learning opportunities throughout your career.
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly.
• Other Employee Benefits:
  • Competitive compensation programs that recognize and reward performance.
  • Comprehensive health, wellness, retirement, and PTO benefits.
  • Office-based culture with occasional work-from-home flexibility for eligible positions after training.
  • Company-sponsored social events.

Please note benefits may vary based on country.