Senior Clinical Data Science Programmer

Icon Strategic Solutions; Teletrabalho; BRL 120.000 - 160.000; Tempo integral

Resumo da oferta

A leading healthcare solutions provider is seeking a Senior Clinical Data Science Programmer to develop and maintain programming solutions for clinical trials. You will collaborate with cross-functional teams and support systems integration, using languages like SAS, R, or Python. The ideal candidate has a bachelor's degree and extensive experience in CDMS programming. This position requires advanced English communication skills and offers the flexibility of remote work.

Qualificações

• Extensive experience in programming for CDMS (EDC systems such as Rave/Veeva).
• Strong problem-solving skills in a fast-paced environment.
• MUST HAVE advanced English communication skills.

Responsabilidades

• Develop, validate, and maintain programming solutions for CDMS.
• Collaborate with various stakeholders to ensure integration of programming solutions.
• Support colleagues in the clinical trials environment.

Conhecimentos

Programming for CDMS

Collaboration

Problem-solving

Attention to detail

Communication

Formação académica

Bachelor's degree in computer science, SAS, statistics or life sciences

Ferramentas

SAS

R

Python

Descrição da oferta de emprego

Senior Clinical Data Science Programmer - Remote - Brazil

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.

What You Will Be Doing

• 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 provide 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.

Your Profile

• Complete bachelor's degree in a 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 skills.

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