Are you a data expert with experience in clinical trials? As a Senior Clinical Data Science Programmer, you will play a crucial role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data.
Main Responsibilities:
* Develop, validate, and maintain programming solutions for CDMS, 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 integration of programming solutions into the overall data management process.
* Serve as the primary point of contact during study setup and maintenance phases for system programming-related questions from the project team.
* Support colleagues with clinical trials environments and concepts of Clinical Data Management Systems.
* Perform extracts of data from CDMS and create data transfer programs.
* Mentor junior programmers and provide guidance on programming best practices, coding standards, and data quality control measures.
* Assist in developing and implementing improvements to technical systems and processes within an SME role.
Key Skills:
* Expertise in programming languages (e.g., Python, R) and data management tools.
* Strong understanding of clinical trials concepts, CDMS, and data management principles.
* Excellent collaboration and communication skills.
* Able to work independently and manage multiple projects simultaneously.
Benefits:
* Opportunity to work on challenging projects and contribute to the growth of the organization.
* Collaborative and dynamic work environment.
* Professional development opportunities.
We are committed to providing a supportive and inclusive workplace. If you are a motivated and detail-oriented individual who is passionate about data science and clinical trials, we encourage you to apply.