Associate Director/Sr. Manager Data Analyst, Statistical Programming

reputed company plc (reputed company: CNTA) new reputed company 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 reputed company the asset-centric model can reputed company to improved reputed company rates for programs with greater speed and modest costs. Description of Role The Associate Director/Sr. Manager Data Analyst in Statistical Programming will reputed company leadership and line management in statistical programming function in one or more therapeutic areas, establish standards for statistical reporting, reputed company and maintain processes to reputed company 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

• reputed company 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 reputed company to programming environments, technology and programming skillset
• Establish and monitor effective and efficient resource management and reputed company 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
• reputed company 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 reputed company 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, reputed company and coach others, reputed company and guide the work of other colleagues to reputed company meaningful reputed company, 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 (Apply tot his job