Senior Biostatistician

Job Description - Senior Biostatistician (2406225957W) Senior Biostatistician-2406225957W Description Johnson & Johnson is currently seeking a Senior Biostatistician to join our Team located in Milpitas, California or Jacksonville, FL. At Johnson & Johnson Vision, we have a bold ambition: to change the trajectory of eye health. That’s why, through our operating companies, we’ve developed solutions for every stage of life—to help people see better, connect better, and live better. We partner with eye care professionals to provide some of the world’s leading products and technologies to address refractive error, cataracts, dry eye, and beyond. We are committed to using our reach and size for good, and strive to put quality eye care within reach of everyone, everywhere. Visit us at www.jjvision.com. Follow JNJVision on Twitter and Johnson & Johnson on LinkedIn. Johnson & Johnson Vision, Clinical Science division has an opening on the Biostatistics team for a Senior Biostatistician, to be located in Irvine CA, or Milpitas CA, or Jacksonville FL. We are seeking a talented and motivated individual who is passionate about clinical trials and statistical research to help meet the unmet needs for vision correction. The Senior Biostatistician provides statistical expertise to plan and complete statistical activities including design, analysis, interpretation, and reporting or communication of data evidence for research, development, and/or marketed product needs in JNJ MedTech, Vision. A pre-identified candidate is being considered for this role. However, all applications will still be considered. Key Responsibilities: This position supports all statistical aspects related to clinical trials, marketing efforts, and research studies for ophthalmology and contact lenses devices. Edits and finalizes statistical analysis plans and system programming plans for all phases of clinical studies and reports on the findings of statistical analyses and publications in preparation for new product applications to regulatory agencies. Demonstrates data analytic expertise based on a foundation of statistical principles related to: design, development and implementation of a clinical trial protocol, clinical database, and/or simulation studies. Open to learn new statistical skills and ready to think out-of-the-box for problem solving solutions including designing simulation studies. Is effective in the use of relevant computational tools for study design or statistical analyses of clinical data. Ensures application of high-quality statistical methods in writing statistical analysis plans and generation of accurate and reproducible statistical analyses of clinical trial outcomes, by working independently and/or in collaboration with colleagues. Design tables/figures/listings and analysis datasets specifications for statistical programmers Produces clear, concise, well-organized, and error-free computer programs and statistical reporting analyses. Ensures that new and revised statistical standards, tests, and processes are implemented for increased accuracy and efficiency Is accountable for execution of project responsibilities including: meetings with project team members, completing statistical deliverables, run a wide range of analyses/graphics. Has very good written, oral, and interpersonal communication skills. Abides by the Credo and practices J&J Leadership Imperatives for Individuals: Lead, Shape, Connect, and Deliver. Proven track record to collaborate with statisticians, data managers and clinical scientists. Qualifications Education: PhD in Statistical Sciences/Biostatistics or related fields (preferred) or Master of Science in Statistics/Biostatistics. Experience and Skills: Required: Overall 1-2 years of experience in clinical trial designs and statistical analysis of clinical data are required, including experience in: drafting Statistical Analysis Plans Editing and reviewing clinical study protocols and reports Quality control of tables/listings/figures and of datasets Some hands-on exposure to innovative study designs or novel analysis methods (e.g. adaptive trials design, meta-analyses or propensity score methods, RWD). Strong skills in SAS and good knowledge of R are required; knowledge of other relevant statistical tools and software is desirable. Knowledge of SDTM and ADaM data structures is required. Open to do intensive SAS programming when needed. Working from one of the company offices either in Milpitas CA, or Irvine CA or Jacksonville FL is required. Preferred: Exposure to or experience with clinical trials for medical devices and/or in the ophthalmology field is preferred. Familiarity with any innovative statistical methodologies such as propensity score methods, or adaptive design features, or Bayesian designs or RWD. Some knowledge of other relevant statistical tools and computer programming languages. Additional Information: The anticipated base pay range for this position is $88,000 to $141,450. California Bay Area - The anticipated base pay range for this position is $103,000. to $165,600. The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis. · Please use the following language: Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Employees are eligible for the following time off benefits: Vacation – up to 120 hours per calendar year Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year Holiday pay, including Floating Holidays – up to 13 days per calendar year of Work, Personal and Family Time - up to 40 hours per calendar year Additional information can be found through the link below. https://www.careers.jnj.com/employee-benefits The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. A pre-identified candidate is being considered for this role. However, all applications will still be considered. Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.