Clinical Data Lead
Há 3 dias
Lead Clinical Data Programmer Role About the Job: We are seeking a highly skilled Clinical Data Programmer to join our team. The successful candidate will be responsible for developing, validating, and maintaining programming solutions for clinical trials. The ideal candidate will have extensive experience in programming for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials with proficiency in languages such as SAS, R, or Python. Key Responsibilities: - Develop, validate, and maintain programming solutions for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials. - Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure the integration of programming solutions into the overall data management process. - Act as a primary point of contact during the study set up and maintenance phase for system programming related questions by the project team. - Support colleagues with the clinical trials environment and concepts of Clinical Data Management Systems. - Perform extracts of data from CDMS and creation of data transfer programs. - Act as mentor and provides guidance and support to more junior programmer levels assigned to a project. - Assist in the development and implementation of improvements to technical systems and processes within an SME role. - Provide guidance on programming best practices, coding standards, and data quality control measures. - Stay updated on advancements in programming languages and data management tools to enhance operational efficiencies. Required Skills and Qualifications: - Bachelor's degree in a relevant field, such as computer science, SAS, statistics, or life sciences. - Extensive experience in programming for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials with proficiency in languages such as SAS, R, or Python. - Strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment. - Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results. - Strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and influence outcomes. - Advanced English Communication, Writing, and Reading skills are required. What We Offer: - Competitive salary and benefits package. - Opportunities for professional growth and development. - Collaborative and dynamic work environment. How to Apply: Please submit your application, including your resume and cover letter, to us.
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Clinical Data Lead
Há 2 dias
Curitiba, Brasil Bebeeclinicaldata Tempo inteiroLead Clinical Data Programmer RoleAbout the Job:We are seeking a highly skilled Clinical Data Programmer to join our team.The successful candidate will be responsible for developing, validating, and maintaining programming solutions for clinical trials.The ideal candidate will have extensive experience in programming for CDMS (EDC systems such as...
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Clinical Data Lead
Há 3 dias
Curitiba, PR, Brasil beBeeClinicalData Tempo inteiroLead Clinical Data Programmer Role About the Job: We are seeking a highly skilled Clinical Data Programmer to join our team. The successful candidate will be responsible for developing, validating, and maintaining programming solutions for clinical trials. The ideal candidate will have extensive experience in programming for CDMS (EDC systems such as...
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Clinical Data Science Program Lead
2 semanas atrás
Curitiba, Brasil beBeeClinical Tempo inteiroSenior Clinical Data Science Programmer This role involves developing and implementing programming solutions to support the analysis and reporting of clinical trial data. Develop, validate, and maintain programming solutions for CDMS, data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials. Collaborate...
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Clinical Data Science Program Lead
2 semanas atrás
Curitiba, PR, Brasil beBeeClinical Tempo inteiroSenior Clinical Data Science Programmer This role involves developing and implementing programming solutions to support the analysis and reporting of clinical trial data. Develop, validate, and maintain programming solutions for CDMS, data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials. Collaborate...
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Lead Clinical Trial Programmer
Há 6 dias
Curitiba, Brasil Bebeeclinical Tempo inteiroSenior Clinical Data Science Programmer Job DescriptionAs 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.Develop and maintain programming solutions for CDMS (EDC systems), data validation outputs, data review/risk...
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Lead Clinical Trial Programmer
1 semana atrás
Curitiba, Brasil beBeeClinical Tempo inteiroSenior Clinical Data Science Programmer Job Description 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. Develop and maintain programming solutions for CDMS (EDC systems), data validation outputs, data review/risk...
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Leading Clinical Projects
4 semanas atrás
Curitiba, Brasil beBeeClinicalProjectManager Tempo inteiroClinical Project Leadership As a clinical project leader, you will ensure that clinical projects are executed within scope, time, and budget. Your role will involve planning, executing, and closing projects while building timelines and managing risks, resources, and milestones. Key Responsibilities: Plan and execute clinical projects to meet scope, time, and...
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Curitiba, PR, Brasil beBeeClinicalProjectManager Tempo inteiroJob Opportunity We are seeking a skilled Clinical Project Manager to lead vaccine projects in LATAM. This role requires flexibility and expertise to deliver projects successfully. Main Responsibilities: Ensure regulatory compliance and oversee cross-functional teams for timely project delivery, quality standards, and budget management. Develop and manage...
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Senior Clinical Research Coordinator
1 semana atrás
Curitiba, Brasil beBeeClinicalResearch Tempo inteiroJob Overview We are seeking a highly skilled Clinical Research Associate to join our team. Key Responsibilities: Clinical trials require meticulous site qualification, initiation, interim monitoring, and close-out visits to ensure accurate data collection and reporting. The CRA will verify that all clinical trial documentation is maintained according to...
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Senior Clinical Research Coordinator
Há 4 dias
Curitiba, Brasil Bebeeclinicalresearch Tempo inteiroJob Overview We are seeking a highly skilled Clinical Research Associate to join our team. Key Responsibilities Clinical trials require meticulous site qualification, initiation, interim monitoring, and close-out visits to ensure accurate data collection and reporting. The CRA will verify that all clinical trial documentation is maintained according to...
