Principal Statistical Programmer

1w1 week ago

Kenvue

Bengaluru, IN · Full-time · INR 3,000,000 – INR 6,000,000

About this role

Kenvue is currently recruiting for a Principal Statistical Programmer. This position reports into Global BioStats, Data Mgmt & Prog and is based at Bangalore with hybrid work location. At Kenvue, we realize the extraordinary power of everyday care with iconic brands including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID®.

Lead and support all programming activities per project strategies, working independently to implement and drive programming for clinical studies, regulatory submissions, and ad hoc/post hoc analysis. Work closely with biostatistics, data management, clinical research, regulatory affairs, and external service providers. Ensure all programming results are delivered in a timely manner with high quality.

Join a global team of ~22,000 brilliant people with a workplace culture where every voice matters and every contribution is appreciated. Passionate about insights, innovation, and committed to delivering the best products to customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day.

Participate in preparation and improvement of relevant standard operating procedures. Provide expert support and direction in statistical programming design for timely and accurate reporting on assigned projects and ad hoc requests. Drive excellence in statistical programming and contribute to clinical development programs for meaningful impact.

Requirements

Expertise in statistical programming for clinical trials and regulatory submissions
Proficiency in implementing project strategies independently
Strong collaboration skills with biostatistics and data management teams
Experience delivering high-quality programming results on time
Knowledge of clinical research and regulatory affairs processes
Ability to develop and improve standard operating procedures
Expert support in statistical programming design and reporting
Familiarity with ad hoc and post hoc analysis in pharmaceutical studies

Responsibilities

Lead and support all programming activities per the project strategies for clinical studies, regulatory submissions, and ad hoc/post hoc analysis
Work independently implementing and driving the programming to support clinical studies
Work closely with biostatistics, data management, clinical research, regulatory affairs, and external functional service providers
Ensure all the programming results are delivered in timely manner with high quality
Participate in preparation and improvement of relevant standard operating procedures
Provide expert support and direction in statistical programming design
Ensure timely and accurate reporting for assigned projects and ad hoc requests
Manage programming activities to support clinical development programs