Clinical Research Associate, Sponsor Dedicated – Italy

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Responsibilities

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- Performing site selection, initiation, monitoring and close‑out visits
- Supporting the development of a subject recruitment plan
- Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
- Collaborating with experts at study sites and with client representatives

Qualifications

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- University Bachelor's Degree and Master's Degree in scientific discipline or health care
- In possession of CRA Certification as required by Ministerial Decree dated 15.11.2011
- Experience in Pharma Industry, and/or Clinical Trials environment




- Very good computer skills including MS Office
- Excellent command of English language
- Organizational, time management and problem‑solving skills
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
- Flexibility to travel
- Driver’s license class B

What You Can Expect

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- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Excellent working environment in a solido, international, reputable company
- Company car, mobile phone and attractive benefits package

Seniority level
Mid‑Senior level

Employment type
Full‑time

Job function
Research, Analyst, and Information Technology

Industries
Hospitals and Health Care

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life scie

📌 Clinical Research Associate, Sponsor Dedicated (Milano)
🏢 Iqvia
📍 Milano