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Overview
Are you ready to shape the future of oncology therapeutics? Join our expanding biotechnology company as we advance groundbreaking treatments. Following our successful Series A funding round, we\'re scaling our team with exceptional talent to accelerate our mission of bringing life-changing therapies to cancer patients worldwide. About the Role
We\'re seeking an Associate Director of Biostatistics to lead statistical strategy across our oncology pipeline. You will be designing and analyzing clinical trials that could redefine cancer treatment standards, working alongside world-class scientists and clinicians in a fast-paced, innovation-driven environment. Responsibilities
Spearhead biostatistical initiatives within our collaborative environment while maintaining focus on critical business objectives Provide statistical expertise and strategic insights for clinical development programs across our oncology portfolio Create cutting-edge study architectures and statistical approaches to address complex oncology research questions Execute comprehensive statistical analyses for early-phase through pivotal trials Develop protocol statistical content, power calculations, randomization strategies, and regulatory documentation Coordinate statistical planning and execution across multiple data streams to support clinical milestones Partner with programming teams to ensure accurate implementation of analysis specifications Manage external statistical service providers and ensure quality deliverable execution Contribute to regulatory strategy and support interactions with global health authorities Mentor and lead juniors to build organizational capability Partner with Data Management teams Qualifications & Experience
Masters Degree or PHD in Biostatistics, Statistics, Mathematics, or related quantitative discipline Minimum 6 years of pharmaceutical or biotechnology industry experience Background in neurology and/or oncology therapeutic development preferred Track record of regulatory agency interactions and submission support highly desirable Advanced proficiency in SAS and/or R for statistical computing, modeling, and data validation Solid understanding of CDISC data standards (SDTM, ADaM) and clinical data structures Experience managing statistical vendors and external partnerships Leadership experience developing statistical talent and driving team performance Strong written and verbal communication skills with strong stakeholder management experience If you\'re passionate about using statistical expertise to advance oncology therapeutics and thrive in a dynamic, growth-stage environment, we\'d love to hear from you. Seniority level
Director Employment type
Full-time Job function
Engineering, Information Technology, and Science Industries
Biotechnology Research and Pharmaceutical Manufacturing
#J-18808-Ljbffr
Are you ready to shape the future of oncology therapeutics? Join our expanding biotechnology company as we advance groundbreaking treatments. Following our successful Series A funding round, we\'re scaling our team with exceptional talent to accelerate our mission of bringing life-changing therapies to cancer patients worldwide. About the Role
We\'re seeking an Associate Director of Biostatistics to lead statistical strategy across our oncology pipeline. You will be designing and analyzing clinical trials that could redefine cancer treatment standards, working alongside world-class scientists and clinicians in a fast-paced, innovation-driven environment. Responsibilities
Spearhead biostatistical initiatives within our collaborative environment while maintaining focus on critical business objectives Provide statistical expertise and strategic insights for clinical development programs across our oncology portfolio Create cutting-edge study architectures and statistical approaches to address complex oncology research questions Execute comprehensive statistical analyses for early-phase through pivotal trials Develop protocol statistical content, power calculations, randomization strategies, and regulatory documentation Coordinate statistical planning and execution across multiple data streams to support clinical milestones Partner with programming teams to ensure accurate implementation of analysis specifications Manage external statistical service providers and ensure quality deliverable execution Contribute to regulatory strategy and support interactions with global health authorities Mentor and lead juniors to build organizational capability Partner with Data Management teams Qualifications & Experience
Masters Degree or PHD in Biostatistics, Statistics, Mathematics, or related quantitative discipline Minimum 6 years of pharmaceutical or biotechnology industry experience Background in neurology and/or oncology therapeutic development preferred Track record of regulatory agency interactions and submission support highly desirable Advanced proficiency in SAS and/or R for statistical computing, modeling, and data validation Solid understanding of CDISC data standards (SDTM, ADaM) and clinical data structures Experience managing statistical vendors and external partnerships Leadership experience developing statistical talent and driving team performance Strong written and verbal communication skills with strong stakeholder management experience If you\'re passionate about using statistical expertise to advance oncology therapeutics and thrive in a dynamic, growth-stage environment, we\'d love to hear from you. Seniority level
Director Employment type
Full-time Job function
Engineering, Information Technology, and Science Industries
Biotechnology Research and Pharmaceutical Manufacturing
#J-18808-Ljbffr