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Há 3 dias

Recife, Brasil beBeeClinical Tempo inteiro

**Job Title:** Freelance Clinical Research Associate Role Overview: In this role, you will lead site visits and ensure high-quality data as a seasoned clinical research professional. Conduct thorough site evaluations and initiations to assess compliance and efficiency Verify GCP compliance and integrity by monitoring data collection processes Collaborate with investigators and internal teams to achieve shared goals Review study protocols and manuals to ensure understanding of project requirements Support site staff with training and issue resolution for seamless operations Track investigational product inventory and documentation accurately Attend investigator meetings and study-related events to stay informed Assist in audit readiness and inspection support to maintain quality standards Your Profile: Minimum 2 years CRA experience with strong site monitoring background Prior IQVIA experience is an asset Demonstrated expertise in clinical trial processes and GCP guidelines Excellent verbal and written communication skills with attention to detail Able to work independently and manage priorities effectively Fluency in English and Portuguese essential About This Opportunity: This freelance position offers flexibility and autonomy, ideal for professionals seeking varied projects and challenges. Key Responsibilities: - Lead site visits to monitor compliance and data quality - Verify GCP compliance and integrity through data review - Collaborate with investigators and internal teams - Review study protocols and manuals - Support site staff with training and issue resolution - Track investigational product inventory and documentation - Attend investigator meetings and study-related events - Assist in audit readiness and inspection support

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    Há 20 horas

    Recife, Brasil Bebeeclinical Tempo inteiro

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    Recife, Brasil beBeeClinicalResearchAssociate Tempo inteiro

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