Principal Statistical Programmer
Opella Healthcare GroupMatch Score
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Protocol Intelligence
Data-driven signals on your job's competitivenessTier-1 pharma brand and metro location increase applicant density despite niche SAS/CDISC skillset.
Clinical trial SAS/CDISC expertise is highly specialized and not easily transferable across industries.
Explicit senior experience plus mandatory SAS/CDISC and clinical trial experience makes filters strict.
Job Description
Structured overview of role & requirementsAbout This Role
Implement and quality control statistical analysis plans and produce data packages (tables, figures, listings) for medical publications and ad-hoc requests.
Develop, implement, and document advanced statistical programming techniques including non-routine macros using SAS.
Collaborate with local and global biostatisticians and programmers and ensure compliance with SOPs, timelines, and quality standards.
Minimum Requirements
Master's degree with minimum 6 years or Bachelor’s degree with minimum 8 years relevant experience in Statistics, Computer Science, Mathematics, Engineering, Life Sciences, or related field.
Advanced SAS programming skills with experience in SDTM & ADaM (CDISC) standards and clinical data environments across multiple therapeutic areas.
Excellent written and spoken English language skills.
Work Experience Required: Minimum 6 years (Master's) or 8 years (Bachelor's) in relevant statistical programming roles.
Ideal Candidate Profile
Experienced in statistical programming and analysis for medical affairs and clinical trial publications within a regulated pharmaceutical environment.
Capable of mentoring and coaching junior team members and supporting onboarding processes.
Able to manage multiple high-priority deadlines independently while maintaining strong stakeholder collaboration and communication.