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Clinical Research Associate, Sponsor Dedicated - Italy

IQVIA

Clinical Research Associate, Sponsor Dedicated - Italy

full-timePosted: Aug 2, 2026Updated: Sep 1, 2026Italy, Milan

Job Description

Experienced Clinical Research Associate, ItalyYour responsibilities will include:Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutionsCollaborating with experts at study sites and with client representativesQualifications:University Bachelor's Degree and Master's Degree in scientific discipline or health careIn possession of CRA Certification as required by Ministerial Decree dated 15.11.2011Experience in Pharma Industry, and/or Clinical Trials environmentVery good computer skills including MS OfficeExcellent command of English languageOrganizational, time management and problem-solving skillsAbility to establish and maintain effective working relationships with coworkers, managers, and clientsFlexibility to travelDriver’s license class BWhat you can expect: Resources that promote your career growthLeaders that support flexible work schedulesPrograms to help you build your therapeutic knowledgeExcellent working environment in a stabile, international, reputable companyCompany car, mobile phone and attractive benefits packageIQVIA 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 population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is €32,200.00 - €53,400.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Locations

  • Italy, Milan

Skills Required

  • Pharma Industryintermediate

Required Qualifications

  • University Bachelor's Degree and Master's Degree in scientific discipline or health care (degree in scientific discipline or health care)
  • In possession of CRA Certification as required by Ministerial Decree dated 15.11.2011 (certification)
  • Experience in Pharma Industry, and/or Clinical Trials environment (experience)
  • Very good computer skills including MS Office (experience)
  • Excellent command of English language (experience)
  • Organizational, time management and problem-solving skills (experience)
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients (experience)
  • Flexibility to travel (experience)
  • Driver’s license class B (experience)

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

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