Clinical Trial Project Manager - Infectious Diseases - Denver

Medpace, Inc.•Denver, CO

39d•Onsite

About The Position

Medpace is hiring a Clinical Trial Project Manager focused on Infectious Diseases to join its Clinical Trial Management Group at the Denver, Colorado office. The role manages day-to-day project operations in accordance with contracts, ICH/GCP, and applicable laws and regulations. It serves as the primary Sponsor contact for operational issues and study deliverables, and provides cross-functional oversight of project teams, vendors, and site quality. The position also involves developing operational plans, managing risks and timelines, and contributing to study documents and deliverables. Medpace is a full-service clinical contract research organization providing Phase I–IV clinical development services. The company describes its work as advancing clinical research to accelerate the development of safe and effective medical therapeutics. This is an office-based role with occasional work-from-home flexibility for eligible positions after training.

Requirements

Bachelor’s degree in a health-related field.
Experience in Phase 1–4 clinical trials.
3–5 years of experience as a project or clinical trial manager within a CRO.
Strong leadership skills.

Nice To Haves

Advanced degree in a health-related field.
Experience in Phase 2–3 clinical trials.

Responsibilities

Manage and provide accountability 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.
Manage the overall project timeline.

Benefits

Competitive salary and bonus program, with potential for bonus and equity awards.
Equity grants.
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 insurance.
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.
On-site mentors.
Defined career paths and advancement opportunities.
Onboarding, training, and ongoing learning opportunities.
Company-sponsored social events.