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Tier-1 employer, Bangalore metro, and mid-level requirement raise competition despite niche SAS/CDISC specialization.
Clinical SAS and CDISC regulatory experience is highly industry-specific and not easily transferable.
Explicit 5+ years plus mandatory SAS/CDISC and clinical/regulatory experience produces strict shortlisting filters.
Lead statistical programming activities in Oncology Biometrics Programming department supporting clinical study reporting, regulatory submissions, and commercialization.
Deliver statistical programming solutions across multiple concurrent clinical studies ensuring accuracy and compliance with technical and regulatory standards.
Collaborate globally and influence stakeholders in clinical drug development to meet study and submission deadlines with high-quality outputs.
Bachelor's or Master's degree in Mathematics, Statistics, Computer Science, Life or Social Sciences, or related field.
At least 5 years of industry experience in statistical programming within pharmaceutical or healthcare, with Master’s or 5+ years with Bachelor’s degree.
Extensive advanced SAS programming expertise and comprehensive knowledge of technical and regulatory requirements in clinical drug development.
Must be able to work hybrid from Manyata Tech Park, Bangalore with minimum 3 days per week onsite.
Experienced in Oncology therapeutic area with expertise in clinical trial programming and submission processes.
Proven ability to lead programming activities or studies with stakeholder management experience in global clinical development.
Strong adherence to CDISC standards and industry best practices ensuring regulatory compliance and data quality.