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Experienced Clinical Research Associate FSP Romania

IQVIA

Experienced Clinical Research Associate FSP Romania

full-timePosted: Aug 6, 2026Updated: Sep 1, 2026Romania, Bucuresti

Job Description

Experienced Clinical Research Associate - Sponsor DedicatedIQVIA Romania is looking for talented and motivated team member to join our Sponsor dedicated team as Senior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.Your 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 representativesYour ProfileUniversity degree in scientific discipline or health careExperience in Pharma Industry, and/or Clinical Trials environment performing independent monitoring for at least 2 years.Very good computer skills including MS OfficeExcellent command of Romanian and English language. Romania based.Organizational, 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/Car Allowance, mobile phone and attractive benefits packagingHome-based role on any part of the country.Candidates who are available to join before October 2026 may be considered for a discretionary sign-on bonus. Eligibility and the bonus amount will be determined on an individual basis, taking into account factors such as role level, experience, skills, and business requirements, and will be confirmed during the offer process.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 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.

Locations

  • Romania, Bucuresti

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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