Staff Statistician, Biostatistics - J&J Vision Care - Jacksonville, FL / Irvine, CA / or Possible Remote US
已发布 2 几个月前
Job DescriptionJohnson & Johnson Vision Care Inc., a member of the Johnson & Johnson Family of Companies, is currently recruiting for a Staff Statistician, Biostatistics to join our Clinical Science division. We are seeking a dedicated and motivated individual who is passionate about clinical trials and statistical research to help meet the unmet needs for vision correction. The primary and preferred location for this position is Jacksonville, FL. Consideration may be given for candidates located near Irvine, CA or those who are Remote within the US.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 Vision on LinkedIn.The Staff Statistician 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 Vision.Responsibilities
This position supports all statistical aspects related to clinical trials, regulatory approvals, marketing efforts, and internal processes initiatives.
Provides guidance on standards and processes and/or technical direction to more junior personnel within the biostatistics group.
Abides by the Credo and practices J&J Leadership Imperatives for Individuals: Lead, Shape, Connect, and Deliver.
Demonstrates advanced data analytic expertise based on a foundation of statistical principles and a track record of applied experience in: design, development and implementation of a clinical trial protocol, clinical database, and/or simulation studies.
Is effective in the use of relevant computational tools for study, or simulations objectives.
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.
Produces clear, concise, well-organized, and error-free computer programs and statistical reporting analyses.
Keep-up with innovation in the statistical sciences by continuous learning of statistical methods to meet business objectives.
Takes a lead in providing support to design, modeling, simulating, analysis planning, execution, interpretation, and statistical communications.
Is accountable for execution of project responsibilities, including: meetings with project team members, presenting to company leaders, run a wide range of analyses/graphics.
Has very good written, oral, and interpersonal communication skills.
Proven track record of collaboration with non-statisticians, translating complex statistical concepts to clinical science and R&D partners.
ORMaster of Science in Statistics/Biostatistics with at least 3 years related hands-on experience with clinical studies protocol and statistical analysis plan documents, clinical trial designs, and statistical analysis of clinical data is required.
Strong experience with SAS and good knowledge of R, as well as knowledge of other relevant statistical tools are required.
Some experience with simulation studies and advanced graphic tools is required.
Some familiarity with at least one area of novel approaches (e.g. meta-analysis, RWD integration, adaptive designs, Bayesian statistics, futility/efficacy stopping rules, etc) is preferred.
Ability to learn sophisticated statistical skills and ready to think out-of-the-box for problem solving solutions is required.
Strong verbal and written communication skills are required, as well as the ability to work cross functionally with various teams is required.
The preferred location for this position is Jacksonville, FL. Consideration may be given for strong candidates who are based in/near Irvine, CA or Remote within the US with the ability to travel 10%-25%.
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. The anticipated base pay range for this position is $102,000 to $163,000. For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits . 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 .https://www.careers.jnj.com/data-science#JNJDataScienceIND7Primary LocationNA-US-Florida-JacksonvilleOther LocationsNA-United States, NA-US-California-Irvine, NA-US-California-MilpitasOrganizationJohnson & Johnson Vision Care, Inc. (6094)Job FunctionBiostatisticsJob QualificationsPhD in Statistical Sciences/Biostatistics or related fields with at least 2 years related hands-on experience with clinical studies protocol and statistical analysis plan documents, clinical trial designs, and statistical analysis of clinical data is required.