Principal Statistical Programmer

Katalyst HealthCares & Life Sciences; Nova Iguaçu; Presencial; BRL 70.000 - 100.000; Tempo integral

Resumo da oferta

A leading company in the healthcare and life sciences sector is seeking a SAS Programmer skilled in clinical trial processes. This role involves collaborating with biostatistical teams, ensuring high-quality programming deliverables, and supporting data management tasks. Ideal candidates will have a strong educational background in relevant fields and demonstrated experience in SAS programming.

Qualificações

• Minimum years of SAS programming experience with clinical trial data.
• Good knowledge of CDISC SDTM and Adam Implementation Guidelines.
• Strong verbal and written communication skills.

Responsabilidades

• Perform SAS programming activities to meet timelines and quality.
• Work with data managers to generate outputs for data cleaning.
• Communicate effectively within Biometrics and with cross-functional teams.

Conhecimentos

SAS programming

Teamwork

Communication

Data analysis

Formação académica

Bachelor's Degree in statistics, computer science or related field

Master's Degree in statistics, computer science or related field

Descrição da oferta de emprego

• Perform SAS programming activities to meet timelines, budget, and quality in accordance with Company study contracts and SOPs.
• Effectively work with Biostatisticians and Statistical Programming team to review data specs, generate or QC analysis datasets and generate or QC analysis outputs per requests for internal medical monitoring, CSR, and submission needs.
• Work with data managers to generate ongoing outputs to support data cleaning and to enhance data integrity.
• Communicate effectively within Biometrics and with cross-functional team members.
• Provide programming expertise to review / QC the programming work provided by the CRO including QC outputs, datasets, and programming related documents; debug programming errors as needed.
• Work on special projects as needed.
• Support internal analysis data and reporting deliverables. Ensure timely, targeted, and accurate reporting and outcomes.
• Develop or QC and document Statistical Programming team macros.
• Ability to work within a team as well as independently.
• Ability to lead a programming deliverable as needed.

Requirements :

• Bachelor's Degree in statistics, computer science or another related science field with a minimum of years of SAS programming experience with clinical trial data OR master's degree in statistics, computer science or another related science field with a minimum of years of SAS programming experience with clinical trial data.
• Good working knowledge of CDISC SDTM and Adam Implementation Guidelines.
• General knowledge of regulatory requirements and drug development process.
• Strong verbal and written communication skills.
• Ability to work independently as well as part of programming teams.
• Strong communication skills set with peers and other group partners.
• Consistently deliver high quality deliverables on time and meet the project delivery expectation.