Senior Clinical Data Science Programmer
As a key member of our team, you will be responsible for developing programming solutions to support clinical trial data analysis and reporting. This includes collaborating with data managers, project managers, and biostatisticians to integrate programming solutions into data management processes. You will also provide guidance on programming best practices, coding standards, and data quality control measures.
Responsibilities:
1. Develop, validate, and maintain programming solutions for CDMS, data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials.
2. Collaborate with team members to ensure integration of programming solutions into overall data management process.
3. Act as primary point of contact during study set up and maintenance phase for system programming related questions.
4. Support colleagues with clinical trials environment and concepts of Clinical Data Management Systems.
5. Perform extracts of data from CDMS and creation of data transfer programs.
6. Assist in development and implementation of improvements to technical systems and processes within SME role.
7. Stay updated on advancements in programming languages and data management tools to enhance operational efficiencies.
Requirements:
* Complete bachelor's degree in relevant field such as computer science, SAS, statistics, or life sciences.
* Extensive experience in programming for CDMS, data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials.
* Strong problem-solving skills and ability to work collaboratively in fast-paced, cross-functional environment.
* Excellent attention to detail and organizational skills, with commitment to delivering high-quality results.
* Strong communication and interpersonal skills, with ability to effectively collaborate with diverse teams and influence outcomes.
* Advanced English Communication, Writing and Reading skills.