Clinical Trial Manager Position

1 semana atrás


Recife, Brasil beBeeClinicalResearchAssociate Tempo inteiro

Clinical Research Associate Role Overview The Contract Clinical Research Associate will be accountable for overseeing and managing Phase 2 Seizure study clinical trials. They must ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol. Conduct site qualification, initiation, interim monitoring, and close-out visits to evaluate and manage sites efficiently. Key responsibilities include: Verify and ensure accurate data collection and reporting through meticulous reviews of site performance. Assess site performance and provide corrective actions if necessary to maintain trial integrity. Qualifications: Bachelor's degree in Life Sciences, Nursing, or a related field providing a solid foundation for this role. At least 2-4 years of experience as a Clinical Research Associate in oncology trials, with preference for Phase 2 experience, allowing individuals to develop expertise in their field. Why This Opportunity? Gain hands-on experience in managing clinical trials, enhancing your skills and professional growth. Develop strong analytical and problem-solving skills through regular assessments and issue resolutions.



  • Recife, Brasil Bebeeclinicalresearchassociate Tempo inteiro

    Clinical Research Associate Role OverviewThe Contract Clinical Research Associate will be accountable for overseeing and managing Phase 2 Seizure study clinical trials.They must ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol.Conduct site qualification, initiation, interim...


  • Recife, PE, Brasil beBeeClinicalResearchAssociate Tempo inteiro

    Clinical Research Associate Role Overview The Contract Clinical Research Associate will be accountable for overseeing and managing Phase 2 Seizure study clinical trials. They must ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol. Conduct site qualification, initiation, interim...


  • Recife, Brasil beBeeClinicalResearch Tempo inteiro

    Senior Clinical Research Associate (CRA) This role offers a unique opportunity to advance care for patients with seizure disorders. About the Position Contract Type: 12 months, with strong potential for renewal based on performance. Experience Required: At least 5+ years of independent monitoring experience. Travel Requirements: Regular site visits across...


  • Recife, PE, Brasil beBeeClinicalResearch Tempo inteiro

    Senior Clinical Research Associate (CRA) This role offers a unique opportunity to advance care for patients with seizure disorders. About the Position Contract Type: 12 months, with strong potential for renewal based on performance. Experience Required: At least 5+ years of independent monitoring experience. Travel Requirements: Regular site visits across...


  • Recife, Brasil Bebeeclinicalresearch Tempo inteiro

    Senior Clinical Research Associate (CRA) This role offers a unique opportunity to advance care for patients with seizure disorders.About the Position Contract Type: 12 months, with strong potential for renewal based on performance.Experience Required: At least 5+ years of independent monitoring experience.Travel Requirements: Regular site visits across...

  • Principal Research Scientist

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    Recife, Brasil beBeeClinical Tempo inteiro

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  • Principal Research Scientist

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    Recife, PE, Brasil beBeeClinical Tempo inteiro

    Job Summary We are seeking a detail-oriented and experienced Clinical Research Associate to monitor and manage clinical trials. The CRA will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol. This position involves collaborating with investigators, site personnel, and cross-functional...


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    Recife, Brasil Bebeeclinicalresearch Tempo inteiro

    Contract Clinical Research AssociateThe ideal candidate for this position will be a detail-oriented and experienced professional with a strong background in clinical research.They will be responsible for monitoring and managing Phase 2 Seizure study clinical trials, ensuring that all tasks are completed efficiently and effectively.The primary...