Clinical Trial Project Manager - Cardiovascular, Renal, Gastrointestinal - Denver

Medpace, Inc.•Denver, CO

115d•Onsite

About The Position

Medpace is hiring an established Clinical Trial Manager or Project Manager to join its Clinical Trial Management Group in the Denver, Colorado office, with a focus on cardiovascular, renal, and gastrointestinal therapeutic areas. The role manages clinical trial project operations and deliverables in accordance with the contract, ICH/GCP, and applicable laws and regulations. The Project Manager serves as the primary sponsor contact for operational issues, provides cross-functional oversight of project teams, manages study risks and vendors, and oversees site quality and monitoring deliverables. The position requires a bachelor's degree in a health-related field and 3–5 years of project or clinical trial management experience within a CRO. Experience across Phases 1–4 is required, with Phases 2–3 preferred. An advanced degree in a health-related field is preferred. The stated target salary range is $100,000–$190,000, with potential bonus and equity awards. Compensation is based on skills and experience. The posting describes an office-based work environment with occasional work-from-home flexibility for eligible positions after training.

Requirements

Bachelor's degree in a health-related field.
Experience in Phases 1–4.
3–5 years of experience as a project or clinical trial manager within a CRO.
Experience managing the overall project timeline.
Strong leadership skills.

Nice To Haves

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

Responsibilities

Manage and be accountable for day-to-day project operations as defined by the contract and in accordance with 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 equity awards.
Medical, dental, and vision coverage.
401(k).
Vacation policy, sick days, and paid holidays.
Work-from-home flexibility for eligible positions.
Short-term and long-term disability.
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.
On-site mentors, defined career paths, onboarding and training programs, and ongoing learning opportunities.
Company-sponsored social events.