Clinical Trial Manager Position
Há 6 dias
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.
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Clinical Trial Manager Position
1 semana atrás
Recife, Brasil beBeeClinicalResearchAssociate Tempo inteiroClinical 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...
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Clinical Trial Manager Position
1 semana atrás
Recife, Brasil Bebeeclinicalresearchassociate Tempo inteiroClinical 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...
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Clinical Research Coordinator
Há 12 horas
Recife, PE, Brasil beBeeClinicalResearch Tempo inteiroSenior 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...
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Principal Research Scientist
3 semanas atrás
Recife, PE, Brasil beBeeClinical Tempo inteiroJob 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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Clinical Research Coordinator
Há 2 dias
Recife, Brasil beBeeClinicalResearch Tempo inteiroSenior 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...
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Senior Clinical Data Science Developer
Há 13 horas
Recife, PE, Brasil beBeeClinical Tempo inteiroSenior Clinical Data Science Programmer Role: We are seeking a highly skilled professional to develop and implement programming solutions for clinical trial data analysis. Develop, validate, and maintain programming solutions for CDMS systems, data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials....
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Senior Clinical Programmer Analyst
2 semanas atrás
Recife, PE, Brasil beBeeClinical Tempo inteiroJob Opportunity: Develop, validate, and maintain programming solutions for clinical trials in the pharmaceutical industry. Key Responsibilities: Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure integration of programming solutions into overall data management process. Act as primary point of contact...
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Principal Research Scientist
2 semanas atrás
Recife, Brasil beBeeClinical Tempo inteiroJob 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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Epilepsy Study Clinical Research Associate
3 semanas atrás
Recife, PE, Brasil beBeeResearch Tempo inteiroSenior Clinical Research Associate We are seeking an experienced Senior Clinical Research Associate to join our team in a Phase II/III Epilepsy Study. The successful candidate will be responsible for conducting site visits across Brazil, ensuring quality and consistency in the execution of the study. This is a 1.0 FTE contract role with a strong chance of...
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Principal Clinical Data Scientist
Há 6 dias
Recife, PE, Brasil beBeeClinical Tempo inteiroKey Programmer Role for Clinical Data Science This position plays a pivotal part in driving innovation and excellence by developing programming solutions for the analysis and reporting of clinical trial data. The role is critical to advancing innovative treatments and therapies. Developing, validating, and maintaining programming solutions Collaborating with...