Clinical Research Associate

1 dia atrás

Recife, Brasil Bebeecoordination Tempo inteiro

Clinical Trial Coordination OpportunityWe are seeking a clinical trials coordinator to lead site visits, monitor compliance, and ensure high-quality data while working with a passionate team in Brazil.Conduct site evaluations, initiations, monitoring & close-outs for Phase 2 and 3 clinical trialsEnsure GCP compliance and integrity of trial dataCollaborate with investigators and internal teams to achieve shared objectivesReview protocols, study manuals, and electronic Case Report Forms (eCRFs)Support site staff with training and issue resolution to maintain optimal operationsTrack investigational product inventory and documentationAttend investigator meetings and study-related events to foster open communicationContribute to audit readiness and inspection support to safeguard the integrity of the trialsYour Ideal Profile:Minimum 2 years experience as a CRA or similar role with site monitoring expertisePrior IQVIA monitoring experience is advantageousStrong knowledge of clinical trial processes and Good Clinical Practice (GCP) principlesExcellent verbal and written communication skills, as well as strong organizational abilitiesAbility to work independently, prioritize tasks effectively, and manage multiple projects simultaneouslyFluent proficiency in both English and PortugueseWhy You'll Thrive in this Role:This opportunity allows you to leverage your clinical research expertise to drive project successYou will have the chance to collaborate with a dynamic team and contribute to the advancement of clinical trialsA competitive compensation package ensures that your hard work and dedication are rewardedLet's Discuss How Your Skills Align with This Opportunity:

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