Clinical Trial Manager - Italy (Milan) - Infectious Disease / Immunology

Medpace, Inc. • Milan, NY

13d • Hybrid

About The Position

Medpace is hiring Clinical Trial Managers for its Clinical Trial Management Group in Milan, Italy, with a focus on Infectious Disease and Immunology. Candidates may continue working in their area of expertise or expand into a new therapeutic area. Remote flexibility may be available after probation for candidates with relevant experience. The role manages clinical study operations and project delivery in accordance with contractual requirements, ICH/GCP, and applicable laws and regulations. It includes sponsor communication, cross-functional oversight, study planning and risk management, vendor management, and oversight of site quality and monitoring deliverables.

Requirements

• Bachelor’s degree in a health or life science-related field.
• Experience in Phase 1–4 clinical trials.
• At least 2 years of Clinical Trial Management experience.
• Experience managing overall project timelines.
• Strong leadership skills.

Nice To Haves

• Advanced degree in a health or life science-related field.
• Experience in Phases 2–3.
• CRO experience.
• Bid defense experience.
• Relevant experience for remote flexibility after probation.

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 directly supervising project Clinical Research Associates and monitoring deliverables.

Benefits

• Competitive compensation and bonus program; equity grants are also mentioned.
• Comprehensive health, wellness, retirement, and PTO benefits, which may vary by country.
• Office-based environment with on-site mentors.
• Defined career paths and advancement opportunities.
• Industry-recognized onboarding and training programs, plus ongoing training and continuous learning opportunities.
• Company-sponsored social events.
• Occasional work-from-home flexibility for eligible positions after training.

What This Job Offers

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