Senior Clinical Data Science Programmer
As a Senior Clinical Data Science Programmer, you will be responsible for developing and implementing programming solutions to support the analysis and reporting of clinical trial data.
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Key Responsibilities:
* Design, 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.
* Provide guidance and mentorship to junior programmers assigned to a project.
* Assist in the development and implementation of improvements to technical systems and processes within an SME role.
* Offer expert advice on programming best practices, coding standards, and data quality control measures.
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Requirements:
* Hold a bachelor's degree in computer science, SAS, statistics, or life sciences.
* Possess 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.
* Demonstrate strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment.
* Display excellent attention to detail and organizational skills, with a commitment to delivering high-quality results.
* Exhibit strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and influence outcomes.
* Must have advanced English Communication, Writing and Reading.