(Associate) Director, Biostatistics

Centessa Pharmaceuticals plc (Nasdaq: CNTA) new kind of pharmaceutical company with a deconstructed R&D environment that prioritizes data driven decision making led by subject matter experts. Centessa is advancing a portfolio of high conviction programs with strong biological validation.Our asset-centric model offers a unique R&D logic that has been applied by single asset companies to improve productivity. This operating model has minimal centralized infrastructure, reduced hierarchy, and exclusive focus on data driven capital allocation. Our teams are uniquely incentivized to expeditiously interrogate key scientific hypotheses. We believe the asset-centric model can lead to improved success rates for programs with greater speed and modest costs.Description of RoleAs the (Associate) Director of Biostatistics, you will provide oversight of clinical development planning and execution across one or more therapeutic areas, primarily for late-phase clinical studies. Reporting to the Executive Director, Biostatistics, you will ensure that statistical strategies and methodologies align with clinical development objectives and regulatory expectations. In this critical role, you will lead the development, execution, and interpretation of statistical analyses, ensuring data quality, analysis integrity, and compliance with regulatory standards. This role requires strong statistical and cross-functional leadership to influence clinical development strategy and decision-making, directly contributing to the success of the company's goals.Key ResponsibilitiesLead biostatistics efforts in a team setting and focus on business prioritiesCollaborate on clinical development plan for one or more molecules to provide biostatistical perspective and insightDetermine innovative study designs, appropriate statistical tests and methods for evaluating and generating statistical hypotheses to meet study and regulatory requirementsAt study level, author and review statistical sections for protocols, statistical power and sample size estimate, randomization schemes, clinical study reports, and regulatory submission documentsLead the planning, organization and analysis of different data sources to enable delivery of the statistical analysis plan and clinical study endpoints for assigned productsWork with cross-functional team to develop ad hoc analysis plans and ensure analyses are performed appropriately by programming staffLead and guide third-party statistical vendors and contractors in the execution of relevant deliverables (eg, TLFs, SAPs, blinding plans)Oversee preparation, conduct, and execution for Data Monitoring Committee meetingsMaintain expertise in state-of-the-art statistical methodologies and statistical analysesCollaborate with Data Management to ensure data integrity and qualityQualificationsPhD in Statistics or Biostatistics10+ years of post-PhD experience applying statistical methods in the pharmaceutical industry.Demonstrated experience supporting late-stage (registrational) trials, including experience with regulatory submissions.Knowledge and experience in neurology and/or oncology therapeutic areas preferredExperience of interacting with regulatory agencies, including FDA and EMA, highly desirableAbility to use SAS and/or R programming languages to perform analyses, conduct statistical modeling, and validate important data derivationsHands-on experience working with CDISC standards and programming based on raw datasets, SDTM, and ADaM datasetsAbility to work in a cross-functional matrix environment, and proactively influence teams with innovative clinical development strategyDemonstrates breadth of diverse leadership experiences and capabilities including: the ability to develop and coach other colleagues to achieve meaningful outcomes and create business impactConsistently demonstrates strong oral and written communication skillsCompensationThe annual base salary range for the Director job level is $190,000.00 to $250,000.00.The annual base salary range for the Associate Director job level is $170,000.00 to $225,000.00.Individual compensation within this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, and job knowledge.In addition to base pay, this role is eligible for a discretionary annual bonus and participation in our equity program, allowing you to share in Centessa's long-term success.Centessa also offers a comprehensive benefits package, which includes a 401(k) plan, company-sponsored medical, dental, vision, and life insurance, generous paid time off, and a health and wellness program.Work LocationThe Director, Biostatistics is a remote role based in the US, with infrequent ( Full-Time, ExemptEEOC Statement: Centessa Pharmaceuticals believes in a diverse environment and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Centessa Pharmaceuticals will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.