Clinical Data Science Lead

Há 8 horas


Rio de Janeiro RJ, Brasil beBeeProgramming Tempo inteiro

Senior Clinical Data Science Programmer We are seeking a highly skilled and experienced programmer to join our team. As a senior clinical data science programmer, you will play a pivotal role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. Key responsibilities include: Developing, validating, and maintaining programming solutions for clinical trials, including CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs. Collaborating with data managers, project managers, clinical data scientists, and biostatisticians to ensure the integration of programming solutions into the overall data management process. Acting as a primary point of contact during the study set up and maintenance phase for system programming related questions by the project team. Providing guidance and support to more junior programmer levels assigned to a project. As a senior clinical data science programmer, you will have the opportunity to work on a variety of projects, collaborate with a talented team of professionals, and stay updated on advancements in programming languages and data management tools.



  • Rio de Janeiro, Brasil beBeeProgramming Tempo inteiro

    Senior Clinical Data Science Programmer We are seeking a highly skilled and experienced programmer to join our team. As a senior clinical data science programmer, you will play a pivotal role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. Key responsibilities include: Developing, validating,...


  • Rio de Janeiro, RJ, Brasil beBeeClinical Tempo inteiro

    Job Title: Senior Clinical Data Science Programmer About the Role: This is a senior-level position that requires expertise in clinical trials data management systems. The ideal candidate will have extensive experience in programming languages such as SAS, R, or Python and be able to develop, validate and maintain high-quality programming solutions. We are...


  • Rio de Janeiro, Brasil beBeeClinical Tempo inteiro

    Job Title: Senior Clinical Data Science Programmer About the Role: This is a senior-level position that requires expertise in clinical trials data management systems. The ideal candidate will have extensive experience in programming languages such as SAS, R, or Python and be able to develop, validate and maintain high-quality programming solutions. We are...


  • Rio de Janeiro, Brasil beBeeClinical Tempo inteiro

    Job Title: Senior Clinical Data Science Programmer About the Role: This is a senior-level position that requires expertise in clinical trials data management systems. The ideal candidate will have extensive experience in programming languages such as SAS, R, or Python and be able to develop, validate and maintain high-quality programming solutions. We are...


  • Santana de Parnaíba, Brasil ICON Strategic Solutions Tempo inteiro

    Senior Clinical Data Science Programmer - Remote - Brazil ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior...


  • Rio de Janeiro, RJ, Brasil beBeeClinicalDataScience Tempo inteiro

    Job Description: This is a key role in the development and implementation of programming solutions to support the analysis and reporting of clinical trial data. The ideal candidate will have a strong background in computer science or a related field, with extensive experience in programming languages such as SAS, R, or Python.

  • Clinical Study Manager

    2 semanas atrás


    Rio de Janeiro, RJ, Brasil beBeeClinical Tempo inteiro

    Contract Clinical Research Associate We are seeking a detail-oriented and experienced professional to monitor and manage Phase 2 Seizure study clinical trials. Main Responsibilities: Site Management: Conduct site qualification, initiation, interim monitoring, and close-out visits. Regulatory Compliance: Ensure all clinical trial documentation is maintained...


  • Rio de Janeiro, Brasil beBeeClinicalDataScience Tempo inteiro

    Job Description: This is a key role in the development and implementation of programming solutions to support the analysis and reporting of clinical trial data. The ideal candidate will have a strong background in computer science or a related field, with extensive experience in programming languages such as SAS, R, or Python.


  • Rio de Janeiro, RJ, Brasil beBeeClinicalResearchAssociate Tempo inteiro

    Job Opportunity: Clinical Research Associate Contract CRA Project - 40 hours per week, 1 year contract. Seizure or Epilepsy - CNS Job Summary: We are seeking a detail-oriented and experienced Clinical Research Associate (CRA) to monitor and manage Phase 2 Seizure study clinical trials. The CRA will ensure the trial is conducted in compliance with regulatory...


  • Rio de Janeiro, RJ, Brasil beBeeClinicalResearchAssociate Tempo inteiro

    Clinical Research Associate Job Description Job Summary: We are seeking a detail-oriented and experienced Clinical Research Associate to monitor and manage Phase 2 clinical trials. The successful candidate will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol. This role involves...