Clinical Research Associate

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 representatives

Qualifications:

University degree in scientific discipline or health careExperience in Pharma Industry, and/or Clinical Trials environmentVery good computer skills including MS OfficeExcellent command of Portuguese and English language.Organizational, time management and problem-solving skillsAbility to establish and maintain effective working relationships with coworkers, managers, and clientsFlexibility to travelDriver’s license class B

What 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 package

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to
accelerate innovation for a healthier world.

We create a culture of belonging by valuing the perspectives of all talented
employees worldwide and providing them with the opportunity to power smarter
healthcare for everyone, everywhere.

When our talented employees bring their authentic selves and their diverse
experiences to work, they enable us to accomplish extraordinary things. Multifaceted
thought processes spark innovation. Multi-talented collaboration harnesses
innovation to deliver superior outcomes.