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

Medpace

Milano

In loco

EUR 60.000 - 85.000

Tempo pieno

30+ giorni fa

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Descrizione del lavoro

A leading clinical research organization in Milan is seeking an experienced Clinical Trial Manager to manage day-to-day project operations. This role includes serving as the primary contact for sponsors, developing project plans, and providing oversight of project deliverables. The ideal candidate has over 5 years of experience in clinical trial management, leadership skills, and a passion for impacting patient lives. The position offers flexible remote work options for qualified candidates.

Servizi

Flexible work environment
Competitive compensation and benefits package
Structured career paths with opportunities for professional growth

Competenze

  • Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred.
  • 5+ years of Project Manager/Clinical Trial Manager experience required for remote role.
  • Bid defense experience preferred.

Mansioni

  • Manage and provide accountability for day-to-day operations of the project.
  • Serve as primary Sponsor contact for operational project-specific issues.
  • Develop operational project plans.

Conoscenze

Clinical Trial Management
Leadership Skills

Formazione

Bachelor’s degree in a health or life science-related field
Advanced degree preferred
Descrizione del lavoro
Job Summary

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in our Milan office. Clinical Trial Managers with expertise in Immunology and Infectious Diseases are welcome to continue to work in their area of expertise or to expand to a new therapeutic area.We provide remote flexibility only with relevant experience (after probation). We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.

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, which includes 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
Qualifications
  • Bachelor’s degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred;
  • Experience in Phases 1-4; Phases 2-3 preferred;
  • Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred;
  • 5+ years of Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based role;
  • Management of overall project timeline;
  • Bid defense experience preferred; and
  • Strong leadership skills.
Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

  • Flexible work environment
  • Competitive compensation and benefits package
  • Competitive PTO packages
  • Structured career paths with opportunities for professional growth
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives

Awards

  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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