IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.
When you join IQVIA Portugal as a sponsor-dedicated CRA, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
With access to world-class training and mentoring, you'll 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.
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 (GCP) and International Conference on Harmonization (ICH) guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study sites and with client representativesQualifications: University degree in scientific discipline or health careAt least 2 years of on-site monitoring experienceGood knowledge of clinical research regulatory requirementsVery good computer skills including MS OfficeExcellent command of Portuguese and 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 knowledgeBetter Work-Life balance, optimal DOSExcellent working environment in a stable, international, reputable companyCompany car, mobile phone and attractive benefits package
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