Clinical Trial Manager - Italy - Neuroscience / Ophthalmology

Medpace, Inc. • Milan, NY

13d • Onsite

About The Position

Medpace is hiring Clinical Trial Managers of different experience levels to join its Clinical Trial Management Group in Italy, particularly at its Milan office. Candidates with Neuroscience and CNS expertise may continue in their area of expertise or expand into a new therapeutic area. Remote flexibility may be available after probation for associates with relevant experience. The role manages clinical study operations and project delivery in accordance with the contract, ICH/GCP, and applicable laws and regulations. It also serves as the primary Sponsor contact for operational project matters and provides cross-functional oversight of internal team members, vendors, sites, and study deliverables.

Medpace is a full-service clinical contract research organization providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. The company reports employing more than 6,500 people across 40+ countries. Its stated mission is to accelerate the global development of safe and effective medical therapeutics through clinical research. The position offers a stated salary range of EUR €56,000–€118,000 per year, along with a competitive salary/bonus program and equity grants. Benefits may vary by country.

Requirements

• Bachelor’s degree in a health- or life-science-related field.
• At least 2 years of Clinical Trial Management experience.
• Experience in clinical trials from Phases 1–4.
• 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.
• Neuroscience or CNS expertise.

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.
• Manage the overall project timeline.

Benefits

• Competitive compensation and bonus programs that recognize and reward performance.
• Equity grants.
• Comprehensive health, wellness, retirement, and PTO benefits.
• Occasional work-from-home flexibility for eligible positions after training.
• Company-sponsored social events.
• On-site mentors.
• Defined career paths and advancement opportunities.
• Industry-renowned onboarding and training programs.
• Ongoing training and continuous learning opportunities.

What This Job Offers

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