Principal Statistical Programmer

1w1 week ago

Kenvue

Bengaluru, IN · Full-time · INR 3,000,000 – INR 5,000,000

About this role

Kenvue realizes the extraordinary power of everyday care, built on over a century of heritage and rooted in science. We're the house of iconic brands including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID®. Science is our passion; care is our talent, with a global team of ~22,000 brilliant people.

The Principal Statistical Programmer leads and supports all programming activities per project strategies for clinical studies, regulatory submissions, and ad hoc analyses. Work independently implementing and driving programming while collaborating closely with biostatistics, data management, clinical research, regulatory affairs, and external providers. Ensure timely delivery of high-quality results.

This role reports to Global BioStats, Data Mgmt & Prog in a hybrid work location in Bangalore. Our workplace culture values every voice and contribution, passionate about insights and innovation. Deliver the best products with expertise and empathy, putting people first.

Participate in preparation and improvement of standard operating procedures. Drive excellence in statistical programming and contribute to clinical development programs. Join us to impact millions daily, shape our future, and yours with brilliant opportunities.

Requirements

Expertise in leading statistical programming for clinical studies and regulatory submissions
Ability to work independently on complex programming implementations
Strong collaboration skills with cross-functional teams including biostatistics and data management
Proficiency in delivering high-quality programming results under tight timelines
Experience in clinical trial data standards and analysis datasets
Knowledge of regulatory requirements for statistical programming outputs
Capability to develop and improve standard operating procedures in biostatistics programming

Responsibilities

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