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Tier-1 pharma brand and Bangalore location increase applicant density, but niche SAS/CDISC skills limit competition.
Role requires domain-specific clinical trial, SAS and CDISC expertise, limiting cross-industry transferability.
Explicit years requirement and mandatory advanced SAS, CDISC, and regulatory experience enforce strict shortlisting.
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Lead and provide statistical programming support for clinical development studies in Oncology, including analysis, reporting, and submissions.
Manage concurrent programming activities ensuring compliance with technical and regulatory standards, particularly for clinical study reports and regulatory submissions.
Collaborate globally and influence stakeholders in Oncology therapeutic area and regulatory submissions to deliver data-driven decisions and support commercialization.
Bachelor's or Master's degree in Mathematics, Statistics, Computer Science, Life or Social Sciences, or related field.
Minimum 3 years industry experience with Master’s degree, or 5+ years with Bachelor’s degree in statistical programming or related pharmaceutical roles.
Advanced SAS programming skills with comprehensive knowledge of clinical drug development and regulatory programming requirements.
Experience leading clinical trial studies or activities and knowledge of CDISC standards; oncology therapeutic area and submission experience preferred.
Experienced in leading multiple clinical programming projects with attention to detail and ability to work independently.
Proficient in stakeholder management and influencing cross-functional teams in a global, hybrid work environment.
Strong domain expertise in Oncology clinical trials with a track record of supporting regulatory submissions and commercialization.