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Strong Tier-1 brand, mid-level 5-8yrs band, and metro Hyderabad increase applicant competition.
High: specialized clinical trial SAS programming and regulatory knowledge limits cross-industry transferability.
Explicit 5-8 years requirement plus mandatory SAS and clinical/regulatory expertise enforces strict filters.
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Lead design, development, and implementation of programming solutions to integrate, analyze, and report clinical trial data.
Provide comprehensive statistical programming support including strategy development, programming standards, specifications, and analysis for clinical project teams.
Collaborate with internal teams and external vendors to ensure quality deliverables, regulatory compliance, and continuous improvement of processes and tools.
Bachelor’s or Master’s degree in statistics, biostatistics, mathematics, computer science, or equivalent experience.
5 to 8 years of clinical/statistical programming experience within pharmaceutical clinical development.
Significant knowledge of SAS software (Base, Stat, Graph), clinical trial methodology, and global regulatory requirements.
Onsite work expectations not explicitly mentioned; no direct supervisory responsibilities.
Experienced in oncology clinical development programming preferred, indicating domain expertise.
Ability to work effectively within cross-functional global teams toward regulatory filings and approvals.
Demonstrated capability in developing programming strategies and contributing to standardization and globalization of processes and tools.