Senior Clinical Data Science Programmer

ICON Strategic Solutions; Mauá; Presencial; BRL 120.000 - 160.000; Tempo integral

Resumo da oferta

A clinical data management firm is seeking a skilled programmer to develop and maintain programming solutions for clinical trials. Responsibilities include collaborating with teams to ensure integration of data management processes and acting as a primary contact for programming-related questions. The ideal candidate will have a relevant bachelor's degree and extensive experience with CDMS systems like Rave or Veeva, along with strong problem-solving and communication skills. Advanced English proficiency is a must.

Qualificações

• Extensive experience in programming for clinical data management systems like Rave and Veeva.
• Strong problem-solving skills and ability to work in a fast-paced environment.
• Excellent communication and interpersonal skills.

Responsabilidades

• Develop and maintain programming solutions for clinical trials.
• Collaborate with cross-functional teams.
• Act as a primary contact for system programming questions.

Conhecimentos

Programming for CDMS

SAS

R

Python

Problem-solving

Communication

Attention to detail

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.