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Programmer leader in clinical trials

Arujá
beBeeClinicalDataScientist
Anunciada dia 13 dezembro
Descrição

Senior Clinical Data Science Programmer Role Summary

We are seeking a Senior Clinical Data Science Programmer to contribute to our clinical trials environment.


Key Responsibilities:

* Develop, validate, and maintain programming solutions for Electronic Data Capture 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 ensure the integration of programming solutions into the overall data management process.
* Act as a primary point of contact during study setup and maintenance for system programming related questions by the project team.
* Support colleagues with the concepts of Clinical Data Management Systems.
* Perform extracts of data from CDMS and creation of data transfer programs.
* Assist more junior programmer levels assigned to a project with guidance and support.
* Develop and implement improvements to technical systems and processes within an SME role.
* Provide guidance on programming best practices, coding standards, and data quality control measures.
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Required Skills and Qualifications:

Excellent programming skills in CDMS systems and experience working with EDC systems such as Rave/Veeva.

Strong collaboration and communication skills to work effectively with cross-functional teams.

Ability to analyze complex data sets and develop creative solutions.

Proficiency in one or more programming languages, including but not limited to Python, Java, C++.

Experience with data validation outputs, data review/risk management outputs, and custom reporting.

Ability to work independently and collaboratively in a fast-paced environment.

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