Lead Clinical Trial Programmer
Há 5 dias
Senior 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 management outputs, custom reports, and programs in clinical trials.Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to integrate programming solutions into the overall data management process.Act as the primary point of contact during study set up and maintenance phase for system programming related questions from the project team.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 QualificationsYou must have a complete bachelor's degree in a relevant field such as computer science, SAS, statistics, or life sciences, along with 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, and strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment.BenefitsThis position offers a unique opportunity to contribute to the advancement of innovative treatments and therapies while ensuring the accuracy and efficiency of data processing through your programming expertise.OthersAs a Senior Clinical Data Science Programmer, you will be working in a dynamic environment where you will have the opportunity to develop your skills and expertise while contributing to the success of our organization.
-
Lead Clinical Trial Programmer
Há 7 dias
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...
-
Clinical Data Lead
1 dia atrás
Curitiba, 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...
-
Clinical Data Lead
1 dia atrás
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...
-
Clinical Data Lead
Há 22 horas
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...
-
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...
-
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...
-
Clinical Trial Manager
1 semana atrás
Curitiba, Brasil NonStop Consulting Tempo inteiroOur client, a growing and developing global CRO, offering a great opportunity and career progression, is hiring a Clinical Trial Manager.Our client is based around the globe and are in search of someone based in Brazil, with a great list of benefits, which include:- Career progression- Open communication- Work in a top rated CRO- Stable environment- To work...
-
Clinical Trial Manager
1 semana atrás
Curitiba, Brasil NonStop Consulting Tempo inteiroOur client, a growing and developing global CRO, offering a great opportunity and career progression, is hiring a Clinical Trial Manager. Our client is based around the globe and are in search of someone based in Brazil, with a great list of benefits, which include: - Career progression - Open communication - Work in a top rated CRO - Stable environment -...
-
Curitiba, Brasil F. Hoffmann-La Roche Gruppe Tempo inteiroAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...
-
Curitiba, Brasil F. Hoffmann-La Roche Gruppe Tempo inteiroAt Roche you can show up as yourself, embraced for the unique qualities you bring.Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.This is how we aim to prevent, stop and cure diseases and ensure everyone...
