Senior Statistical Programmer, R, RShiny

Posted Aug 21

This is a fully remote position, open to applicants in Spain, +2 more countries.

πŸ“‹ Description

β€’ Utilize R/RShiny or similar software to create custom programming code for summary tables, data listings, graphs, and derived datasets.

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

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

β€’ Keep project team members updated on programming advancements and challenges.

β€’ Adhere to relevant SOPs, WIs, and regulatory guidelines such as ICH.

β€’ Maintain comprehensive, up-to-date project documentation, testing, and quality-control records.

β€’ Manage timelines and priorities across multiple projects effectively.

β€’ Create specifications for datasets and outputs of varying complexity.

β€’ Proactively identify and address programming challenges and define variables for peer review and sponsor/requestor acceptance.

β€’ Organize and lead internal meetings, disseminate information and minutes, and ensure action items are completed.

β€’ Provide assistance with projects and initiatives as required.

β€’ Establish time estimates and execute study programming tasks within designated timeframes.

β€’ Serve as the lead statistical programmer and supervise other programming staff.

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 review, constructive feedback, and guidance.

β€’ Transfer deliverables efficiently.

β€’ Execute other assigned work-related tasks.


⛳️ Requirements

β€’ Possess an advanced degree in Statistics, Computer Science, or a related discipline.

β€’ Have extensive experience in statistical programming within a clinical or pharmaceutical environment.

β€’ Familiarity with CDISC programming (SDTM, ADaM) is essential.

β€’ Experience with clinical trials and biomarker analyses is required.

β€’ Demonstrate proficiency in R and RShiny.

β€’ Have a strong grasp of statistical methods and data analysis techniques.

β€’ Exhibit excellent problem-solving and analytical abilities.

β€’ Capability to work autonomously as well as collaboratively in a team setting.

β€’ Possess strong communication and interpersonal skills.

β€’ SAS Certified Advanced Programmer for SAS 9 or an equivalent certification is preferred.

β€’ Consideration will also be given to equivalent experience, skills, and/or education.


🏝️ Benefits

β€’ Opportunities for career development and advancement.

β€’ Supportive and engaged management team.

β€’ Technical and therapeutic area training available.

β€’ Recognition from peers.

β€’ Comprehensive total rewards program.

β€’ Commitment to an inclusive culture.

β€’ Access to extensive resources including emerging technologies, data, science, and knowledge sharing.

β€’ Opportunities for diverse career paths and progression.

β€’ Minimal travel may be required.

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