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Tier-1 pharma brand, Bangalore metro, mid-level experience, and visible senior biostatistics role drive medium competition.
Highly industry-specific biostatistics and regulatory trial experience limits cross-industry transferability.
Senior regulated clinical statistics role requiring PhD/MSc, pharma experience and R/SAS mandates strict filtering.
Lead statistical work for projects or indications including complex studies, ensuring quality and timely delivery either in-house or with CRO partners.
Analyze, interpret, and present clinical study results and develop study design options to support informed business decisions.
Mentor and direct statistical staff and oversee multiple studies within projects focusing on regulatory and technical standards.
MSc or PhD in Statistics, Biostatistics, or equivalent.
5+ years of pharmaceutical industry experience, including program design and data analysis, preferably with Phase III Oncology studies.
Strong knowledge of R and/or SAS programming and experience conducting simulations.
Location: Bangalore with hybrid work arrangement.
Experienced statistical leader capable of independently managing complex clinical projects and therapeutic areas.
Expert in applying advanced statistical modeling and novel approaches aligned with regulatory requirements.
Skilled in collaborating across functional boundaries and mentoring statistics staff in a pharmaceutical development context.