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Protocol Intelligence
Data-driven signals on your job's competitivenessTier-1 brand and Bengaluru location increase competition, but niche clinical SAS specialization reduces applicant pool.
Clinical statistical programming is highly domain-specific to pharma/biotech, limiting cross-industry transferability.
Highly specific regulatory SAS, SDTM/ADaM and clinical trial experience create strict shortlisting filters.
Job Description
Structured overview of role & requirementsAbout This Role
Own programming activities for clinical trial data analysis, including creation of SDTM and ADaM datasets and generation of tables, listings, and graphs.
Collaborate with statistical colleagues on analysis plans, conduct peer reviews, and assist in communication of study results for regulatory submissions and manuscripts.
Maintain and apply proficiency in SAS programming and statistical methodologies; ensure compliance with regulatory and corporate policies.
Minimum Requirements
Proficiency in SAS programming and clinical trial data analysis methodologies (SDTM and ADaM).
Experience with preparation of statistical analysis plans and data quality assurance in clinical trials.
Work Experience Required: Not explicitly mentioned in the JD.
Not explicitly mentioned: mandatory degree, notice period, or specific onsite/location requirements.
Ideal Candidate Profile
Experienced in clinical trial statistical programming with ability to select and justify appropriate statistical methods.
Capable of collaboration across statistics and data management teams, including peer review and communication with regulatory bodies.
Familiarity with therapeutic areas to enhance customer focus and adapt to applicable tools and systems.