Associate Director/Sr. Manager Data Analyst, Statistical Programming Position Available In Suffolk, Massachusetts

Associate Director/Sr. Manager Data Analyst, Statistical Programming
Boston, MA Full Time Posted by:

Centessa Pharmaceuticals, LLC Posted:

Wednesday, 18 June 2025 Associate Director/Sr. Manager Data Analyst, Statistical Programming COMPANY 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 Role The Associate Director/Sr. Manager Data Analyst in Statistical Programming will provide leadership and line management in statistical programming function in one or more therapeutic areas, establish standards for statistical reporting, develop and maintain processes to provide high-quality data analysis, compliance with regulatory standards and efficient execution of programming deliverables, contribute to clinical development planning and execution for multiple indications at Centessa. Key Responsibilities Lead statistical programming efforts in a team setting and focus on business priorities
Collaborate with cross-functional team on clinical study planning and execution to ensure accurate data reporting
Ensure quality and timeliness of statistical analysis, reporting, and regulatory submission deliverables
Demonstrate strong technical expertise and promote best practices related to programming environments, technology and programming skillset
Establish and monitor effective and efficient resource management and capacity development in support of business objectives
Manage and mentor statistical Data Analyst teams, providing guidance and training
Ensure compliance with CDISC standards (SDTM, ADaM) and regulatory requirements
Oversee the development of tables, listings, and figures (TLFs) for clinical study reports Qualifications Advanced degree preferred. 10+ years of relevant work experience in biopharmaceutical, biotech, or CROs industry, with early (Phase 1 and Phase 2) and late (registrational) trial experience highly desired
Solid experience with reporting processes, regulatory requirements, and software development life cycle
Expertise in SAS programming and knowledge of R or Python is a plus
Hands-on experience working with CDISC standards and programming based on raw datasets, SDTM, and ADaM datasets
Demonstrates strong communication skills, both oral and written
Ability to work in a cross-functional matrixed environment, and proactively influence teams with innovative clinical development strategy
Demonstrates breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes, and create business impact Work Location The Associate Director/Sr. Manager Data Analyst, Statistical Programming is a remote role based in the US, with infrequent (