Principal Biostatistician

Principal Biostatistician

What we do

At Kenvue, we realize 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® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours.

Role reports to:

Global BioStats, Data Mgmt & Prog

Location:

Asia Pacific, India, Karnataka, Bangalore

Work Location:

Hybrid

What you will do

Who we are

At Kenvue, we realize 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® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact the life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours.

Principal Biostatistician manages the operations of the biostatistics functions of the department, including activities related to the design and analysis of clinical trials, data submission and ensure the project success, support the data interpretation and date reporting activities and publication strategy.

Responsibilities will include but not limited to

• Collaborate with resources from functional organizations and outside sources to ensure project success.
• Function as Lead Subject Matter Expert (Lead SME) with respect to application of statistical techniques, with related responsibilities governed by applicable procedures.
• Support the design and analysis of clinical trials. Provide oversight of statistical activities at the project level.
• Ensure compliance with all statistical analysis and reporting procedures.
• Participate in sponsor oversight of Biostatistics vendor activities.
• Assist clinical investigators with biostatistics work and the creation of publications and manuscripts.
• Provide support for interactions with and submissions to regulatory agencies.

Required Qualifications

• Graduate degree in Statistics or a related quantitative field with sufficient concentration in statistics
• Typically requires 4+ years of industry experience with PhD degree or equivalent, and 6+ years of industry experience with MS degree or equivalent
• Physical Demands: Office setting. Travel < 15%.
• Pharmaceutical industry experience in clinical development biostatistics methods and processes
• SAS programming experience.
• Excellent oral and written communication skills, and strong interpersonal skills
• Excellent problem-solving skills
• Effective collaboration in cross-functional teams
• Serve as role model for making Credo-based decisions
• Support, influence, or create a trusting, collaborative, and ethical work environment
• Maintain the highest standards of ethics, quality, compliance, and accountability
• Maintain awareness of the external environment, adding value and insights
• Use insights to uncover important unmet needs
• Encourage and support internal collaboration across levels, creating effective solutions
• Contribute to innovative and viable products, services, and/or solutions, adding value
• Challenge the status quo, and adapt to change
• Identify and communicate meaningful risks, and take appropriate action
• Take accountability for own performance and development of self, and support talent acquisition and others' development
• Leverage diverse perspectives, backgrounds, and talent to generate effective ideas or solutions
• Engage in transparent and constructive conversations
• Act with speed, agility, and accountability
• Make effective decisions and take actions based on how work impacts the enterprise
• Manage priorities effectively to deliver expected results

Competencies

• Solid statistical background, with application to clinical trials preferred
• Scientific curiosity, eagerness to grow in statistical knowledge and

applications

• Excellent team player
• Excellent communication skills

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.