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Lead clinical trial programmer

Curitiba
beBeeClinical
Anunciada dia 18 dezembro
Descrição

Senior 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 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 Qualifications

You 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.


Benefits

This 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.


Others

As 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.

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