Clinical Research Associate, Sponsor Dedicated – Italy
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Responsibilities
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
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
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 sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and populatio

Clinical Research Associate, Sponsor Dedicated

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