Statistician

Role Description We are seeking a highly motivated individual to join a recently formed Non-Clinical and Diagnostics Statistics group with experience in one or more areas of experimental design, regression, multivariate, AI, quality control, Bayesian methods and simulation.  The qualified applicant will work broadly across the company in diagnostics and device development, analytical chemistry, pharmaceutical development, discovery and biomarker development and CMC. The successful candidate will work in close partnership with laboratory scientists, engineers, and others to develop and implement fit-for-purpose study designs, experimental plans and analyses to enable robust data-driven decision making and timely delivery of project objectives.  Willingness to understand laboratory methods, device, vaccine and biopharmaceutical development, discovery and biomarker development, and CMC processes in order to better communicate, partner with and educate colleagues is essential. The candidate will be expected to lead statistical aspects of discovery and development activities spanning diverse teams at various stages including product discovery, development, devices, validation, and commercialization.  They will also provide guidance on data collection and retrieval and may need to work with teams to develop systems/programs to allow individual scientists to generate their own visualizations and analyses where appropriate. The colleague will need to also support submission related activities spanning non-clinical development processes such as, but not limited to, assay and process development/validation, specifications.   Our department is highly collaborative, and colleagues are expected to actively participate in group meetings and follow standard departmental procedures. The successful candidate must have excellent communication skills, the ability and desire to work with large, complex teams of scientists, and have the ability to work across multiple projects simultaneously.  This role requires cross site support and occasional travel may be required. Education: PhD in Statistics (or related field with extensive training in statistical methods), preferably with 6+ years industry experience MS in Statistics (or related field with extensive training in statistical methods) with 10+ years of industry experience Essential Skills and Attributes: Knowledge of data handling, statistical analysis and programming in PC-SAS, JMP and R Experience with, but not limited to, statistical design and analysis of experiments, QbD, assay/process validation, data visualization.  Experience working in, but not limited to, one or more areas in developing/validating: medical devices, pharmaceutical products, assay technologies (e.g., PCR, genetic assay technologies, HPLC, etc), robust processes, and robust formulation. Experience and a desire to mentor and coach early in career peers. Experience leading teams through complex issues to address business needs Excellent oral and written communication and statistical consulting skills Ability to critically review scientific publications Highly organized, able to manage multiple simultaneous projects and significant attention to detail Works well in a team environment and consistently follows standard operational practices Champion the use of established and innovative statistical methods across the entire organization Desire and curiosity to learn about the science and business. Desirable Skills and Attributes: Direct experience with statistical aspects of diagnostics kit development and validation in addition to a strong understanding of regulatory considerations in the diagnostics space is highly desirable Knowledge and/or experience with CMC regulatory requirements for diagnostic and/or pharmaceutical products. Regulatory interaction experience (e.g., submissions, audits, inspections, responses)  The US base salary range for this full-time position is $ 128,000 - $177,000 . Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the base pay target range for new hire salaries for the position. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. This position is also eligible for short-term incentive compensation. This position is also eligible for long-term incentives. In addition to compensation, Zoetis offers a comprehensive benefits package that supports the physical, emotional and financial wellbeing of our colleagues and their families including healthcare and insurance benefits beginning on day one, a 401K plan with a match and profit-sharing contribution from Zoetis, and 4 weeks of vacation. Visit zoetisbenefits.com to learn more. Full time   Regular   Colleague   Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Notice: Zoetis Recruiters will contact candidates via email from an address ending in @zoetis.com and may also initially connect with candidates through LinkedIn , including LinkedIn InMail. Zoetis does not use Gmail, Outlook, Yahoo, or other web-based/generic email domains to communicate about job opportunities, interviews, or offers of employment. If you receive a recruitment-related email message claiming to be from Zoetis that