Senior Clinical Data Science Programmer

ICON Strategic Solutions; Aquiraz; Presencial; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A leading specialist in clinical data management in Brazil is looking for a skilled programmer to develop and maintain solutions for CDMS. The successful candidate will collaborate closely with project managers and data scientists and will play a key role in ensuring the integration of programming solutions into clinical trial processes. The ideal applicant will have a relevant bachelor's degree and extensive experience in clinical data management programming, with advanced English communication skills and a keen eye for detail.

Qualificações

• Bachelor's degree in a relevant field such as computer science, SAS, statistics, or life sciences.
• Extensive experience in programming for CDMS, data validation outputs, and clinical trials.
• Strong problem-solving skills and ability to work collaboratively.

Responsabilidades

• Develop and maintain programming solutions for CDMS in clinical trials.
• Collaborate with data managers and project teams on programming solutions.
• Act as a mentor and guide junior programmers on projects.

Conhecimentos

Programming in SAS

Programming in R

Programming in Python

Data validation

Attention to detail

Collaboration

English communication

Formação académica

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

Descrição da oferta de emprego

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 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.

Your Profile

• 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.