Associate Director, Biostatistics
Hyderabad, INPosted Jun 22, 2026
Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsAssociate Director, BiostatisticsHyderabad - TS - IN No longer accepting applications.Job IDR1601655Date posted04/22/2026DepartmentCell TherapyKey Responsibilities·Collaborates in design of innovative and efficient clinical trials, including the selection of study population/endpoints to address study objectives, and contributes to project development strategy·Defends protocols and analysis plans at internal governance reviews and provides independent reviews of complex protocols.·Independently authors and/or reviews protocol, statistical analysis plan, clinical study reports, associated publications, and other study level documents·Presents summary data and analyses results, in a clear, concise, complete, and transparent manner.·Provides statistical support and leadership to address health authority request, publication, presentation, and other public release of information·Manages multiple studies to ensure consistency and adherence to standards within an indication or therapeutic area.·Applies extensive knowledge of statistical / clinical trials methodology as it relates to clinical development.·Invests in developing knowledge outside of traditional statistical expertise in the clinical, regulatory and commercial environments with demonstrated application to study design.·Effectively engages as a matrix team member on project teams, to act as a scientific and strategic partner in the drug development process.·Compliant with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable.·Contributes to external and internal statistical community of practiceDevelops & advises team membersEffectively communicates the GBDS Mission and Vision in a fashion that generates pride, excitement and commitment within GBDS.Enables a culture of inclusiveness, respect for diversity, compliance with process and allows for the questioning and challenging of others in a respectful and constructive manner.Applicable to people managers Effectively engages as an employee advocate and management coach/mentor to team members - both internally and externallyProvides leadership to empower and develop the team.Provides guidance to employee's development plans and carries out performance review and feedback. develops performance metrics for staff.Qualifications & ExperiencePhD (6+ years’ experience) or MS (8+ years’ experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experienceProficiency in scientific computing/programming (SAS, R or Python) and implementation of advanced statistical analysis, data manipulation, graphing & simulation.Great interpersonal, communication, writing and organizational skillsExpertise in statistical/clinical trials methodology as it related to clinical development and ability to apply to relevant clinical development frameworkGood understanding of regulatory landscape and experience with participating in regulatory interactions.Demonstrate collaboration, organizational/ leadership abilities, and interpersonal skillsDemonstrate ability to plan,...