Senior Statistical Programmer – Clinical Trials, SAS, R

Posted Oct 20

This is a fully remote position, open to applicants in Brazil.

πŸ“‹ Description

β€’ Utilize SAS or alternative software to create custom programming code for summary tables, data listings, graphs, and derived datasets in accordance with statistical analysis plans and programming specifications.

β€’ Ensure that outputs adhere to quality standards and project requirements.

β€’ Conduct validation programming and address discrepancies in collaboration with Programmers, Biostatisticians, and project team members.

β€’ Maintain comprehensive and up-to-date project documentation, as well as testing, verification, and quality-control materials.

β€’ Oversee schedules and priorities across multiple projects while adjusting workload to accommodate shifting timelines.

β€’ Formulate specifications for datasets and outputs of varying complexities.

β€’ Prepare for and facilitate internal meetings, distribute information and meeting minutes, and monitor action items.

β€’ Estimate and fulfill study programming tasks within designated timelines.

β€’ Serve as the lead statistical programmer and guide the programming efforts of other team members.

β€’ Review Statistical Analysis Plans, mock shells, programming specifications, annotated CRFs, and SAS database designs.

β€’ Represent statistical programming in sponsor, kickoff, and bid defense meetings.

β€’ Mentor programming staff through training, work evaluations, feedback, and guidance.

β€’ Transfer deliverables and undertake other assigned work-related responsibilities.


⛳️ Requirements

β€’ Bachelor's degree, ideally in a scientific or statistical field; alternatively, an equivalent mix of education and proven programming experience.

β€’ Significant programming expertise in SAS or other required software, ideally within a clinical trial context.

β€’ Outstanding written and verbal communication abilities.

β€’ Proficiency in reading, writing, speaking, and understanding English.

β€’ Experience in the realm of clinical trials.

β€’ Capability to develop statistical programming code and conduct validation programming.

β€’ Familiarity with relevant SOPs, WIs, and regulatory guidelines, including ICH.

β€’ Competence to lead statistical programming endeavors and oversee other programming personnel.


🏝️ Benefits

β€’ Opportunities for career development and advancement.

β€’ Supportive and engaged management.

β€’ Technical and therapeutic area training provided.

β€’ Peer recognition and a comprehensive rewards program.

β€’ An inclusive organizational culture.

β€’ Minimal travel may be necessary.

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