Principal Scientist, Biostatistics
Johnson & Johnson Innovative Medicine
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Benefits offered by this job
Job summary
Johnson & Johnson Innovative Medicine seeks a Principal Scientist, Biostatistics to guide study design, execution, and data interpretation across Clinical Development, Medical Affairs, and Manufacturing Sciences at Spring House, PA or Raritan, NJ.
The role emphasizes leadership in statistical methods, cross-functional collaboration, and advancing quantitative sciences with QSCP, delivering high-quality outputs and influencing regulatory considerations.
Qualifications
- Master's degree with 6+ years of relevant experience or PhD with 4+ years.
- Proficiency in SAS, R, and Python.
- Strong interpersonal and written communication skills.
Responsibilities
- Provide input to design and execution of studies across programs.
- Lead statistical analyses, interpretation, and reporting of data.
- Collaborate with QSCP and other scientists to support drug development.
- Apply high-quality statistical methodologies to projects.
- Lead study design optimization and sample size planning.
Skills
Education
Tools
Job description
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Data Analytics & Computational Sciences
Biostatistics
Scientific/Technology
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
The Principal Scientist provides input to the design and execution of studies and experiments for Clinical Development, Medical Affairs, Discovery, and Manufacturing Sciences programs at J&J Innovative Medicines (J&J IM), with minimal supervision. Support is provided to statistical analysis, interpretation, and reporting or communication of data evidence towards programs for research, development, and/or marketed product needs in J&J IM.
This individual will collaborate with Quantitative Sciences & Clinical Pharmacology (QSCP) functions and other drug development scientists to support statistical aspects of key business and regulatory commitments, contributes to program plans, and represents Statistics & Decision Sciences (SDS) in various teams or working groups. They will practice J&J leadership principles and values aligned with the company’s Credo and purpose.
- Exhibiting advanced proficiency in data analytics, grounded in statistical principles with a proven record of effectively supporting programs.
- Demonstrating competence in using pertinent computational tools for research objectives related to studies, experiments, or trials, including full proficiency in R and SAS, along with familiarity with other relevant computational tools, including innovative data-adaptive methods and artificial intelligence.
- Ensuring the application of high-quality statistical methodologies in assigned projects, showcasing an understanding of the disease/scientific/functional area and compliance with health authority standards.
- Integrating quantitative sciences with disease or functional area requirements, balancing scientific and business needs.
- Providing leadership in optimizing study designs to meet objectives, and supports scenario simulations and sample size calculations informed by technical and area specific knowledge.
- Proactively identifying complexities related to scientific, statistical, regulatory, operational, and partnership aspects. Progresses to more complex programs upon mastering standard ones.
- Identifying and implementing advanced statistical techniques to address complex project or program features.
- Serving as a recognized leader, offering guidance to the team on optimizing study or trial designs in accordance with study or indication level objectives.
- Improving inferential insights while minimizing time, cost, and study risk.
- Collaborating cross-functionally to identify and resolve issues.
- Engaging in process improvement and standards development initiatives.
- Building cross-functional partnerships with internal colleagues and external partners (e.g., Contract Research Organizations (CROs), consultants) to achieve results for project-specific needs, focusing on enhancing communication, efficiency, and productivity.
- Working within SDS and QSCP for unified and integrated quantitative input in drug development.
- Delivering high-quality and timely outputs as evaluated by partners such as the project team, clinical trial team, and the Statistics Area Head.
- Identifying vital external scientific and statistical trends, driving the advancement of statistical methodologies through scholarly publications.
- Participating in interactions with health authorities.
- A minimum of a Master's degree with 6+ years of relevant experience, or a PhD with 4+ years of relevant experience is required.
- Proficiency in SAS, R programming or other relevant computational tools (e.g., East Horizon, RPACT, FACTS, Python) are required.
- Excellent interpersonal, verbal, and written communication skills are required.
- Demonstrated ability to work in interdisciplinary contexts outside statistics is required.
Johnson & Johnson is an 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, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.
If you are under 18 years of age, you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent’s consent for the background check.
$117,000.00 - $201,250.00
Subject to the terms of their respective plans, employees are 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.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period10 days
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
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