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Senior Clinical Data Science Programmer
Job summary
A leading healthcare intelligence organization is seeking a Senior Clinical Data Science Programmer to join their remote team based in São Paulo, Brazil. In this role, you will develop programming solutions for clinical trials, ensuring data accuracy and efficiency. The ideal candidate will possess a Bachelor's degree and extensive experience with CDMS programming using SAS, R, or Python. Strong problem-solving and communication skills are essential for successful collaboration with diverse teams. Advanced English proficiency is a must.
Qualifications
- Bachelor's degree in a relevant field.
- Extensive experience in programming for CDMS and proficiency in SAS, R, or Python.
- MUST HAVE advanced English communication skills.
Responsibilities
- Develop programming solutions for CDMS and clinical trial data.
- Collaborate with cross-functional teams for data management.
- Act as a primary contact for programming-related questions.
Skills
Education
Tools
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development
We are currently seeking a Senior Clinical Data Science Programmer to join our diverse and dynamic team. As a Senior Clinical Data Science Programmer at ICON, you will play a pivotal role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. You will contribute to the advancement of innovative treatments and therapies by ensuring the accuracy and efficiency of data processing through your programming expertise.
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.
Complete bachelor’s degree relevant field such as computer science, SAS, statistics, or life sciences.
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 with proficiency in languages such as SAS, R, or Python.
Strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment.
Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results.
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
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.