Associate Principal Scientist, Statistical Programming

Associate Principal Scientist, Statistical Programming – Rahway, NJ Provide high quality statistical programming analysis and reporting deliverables for global PK modeling and simulation stakeholders within the Oncology therapeutic area. Responsibilities Gather and interpret user requirements, retrieve the required data, transform the data into modeling‑ready analysis datasets, and develop tables and figures according to the modeling analysis plans. Lead the data stewardship and take accountability for the creation of modeling data from original data source(s) to final modeling dataset. Act as a key collaborator with modelers, statisticians and other project stakeholders, executing project plans efficiently and overseeing the work of other team members when opportunities arise. Programmatically synthesize preclinical/clinical data into analysis‑ready structures from varied data sources. Create modeling‑ready datasets by integrating PK, PD and covariate data. Produce tables and graphics for inclusion in study reports and regulatory submissions. Ensure programmatic traceability from data source to modeling result. Support the development of programming standards to enable efficient and high‑quality production of programming deliverables. Produce SAS transport files and associated documentation for regulatory submissions. Represent statistical programming on process improvement activities. Education Requirements Must have a Bachelor's degree (or US equivalent) in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering, Pharmaceutical Sciences, or related field plus 9 years of SAS programming experience in a clinical trial environment. OR Master's degree (or US equivalent) in a related field plus 7 years of SAS programming experience in a clinical trial environment. Position Requirements Significant expertise in SAS and clinical trial programming, including data steps, procedures, SAS/MACRO, SAS/GRAPH; and programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data, derived PK parameters). Ability to design and develop complex programming algorithms; to efficiently manipulate clinical trial datasets including complex data preprocessing, filtering, and manipulation; demonstrated ability to work in an exploratory environment, handling non‑standard data in a variety of formats with minimal requirements. Knowledge of pharmaceutical development processes. Ability to comprehend analysis plans that describe methodology to be programmed. Understanding of statistical or pharmacokinetic terminology and concepts; and ability to implement statistical methods not currently available through commercial software packages. Broad knowledge and significant experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings). Ability to lead at a program level; determine approach, ensure consistency, and direct development of others when opportunities arise; engage key stakeholders. Strong project management skills, excellent interpersonal skills, ability to negotiate and collaborate effectively, and excellent written, oral, and presentation skills. Benefits We offer a comprehensive package of benefits, including medical, dental, vision, retirement benefits, paid holidays, vacation, and compassionate and sick days. Eligible employees may also receive annual bonuses and long‑term incentives. Equal Employment Opportunity As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. #J-18808-Ljbffr