Principal Biostatistician

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在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。

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我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.

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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. For more information, click here.

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

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