Director, Oncology Epidemiology

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at

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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 & Johnson Innovative Medicine is seeking a Director Oncology Epidemiology to join our Global Epidemiology team. The preferred location for this position is either Raritan NJ Titusville NJ or Horsham PA. Consideration may also be given for Spring House PA or Cambridge MA. (No fully remote option.)

The Director Oncology Epidemiology is accountable for working independently while functioning under the supervision of more senior members of Global Epidemiology. The Director Oncology Epidemiology is responsible for oversight of various projects and initiatives in areas of epidemiology and real-world evidence research. This includes leading research projects drafting protocols and statistical analysis plans overseeing the analysis of real-world data (including but not limited to insurance claims data hospital billing data EMRs curated oncology datasets registries) and the dissemination of scientific information through technical reports presentations and publications in peer-reviewed literature.

Additional responsibilities include:

• Identify research study needs drafting proposals and protocols and contribute to real-world evidence (RWE) strategy and study conduct across the therapeutic area portfolio.
• Work closely in collaboration with colleagues in the Epidemiology group when defining research questions developing epidemiological protocols conducting analyses and interpreting and communicating evidence to internal and external stakeholders.
• Participate in various multi-disciplinary matrix teams to address issues raised by product teams/regulatory agencies where real-world data (RWD)/RWE can inform decisions.
• Provide epidemiological and/or statistical consulting and support to compound/product teams and disseminate technical information through reports presentations and publications in peer-reviewed literature as agreed by the team.
• Work within and outside of existing electronic databases to: assess feasibility of fit-for-purpose RWD; research natural history of diseases to understand background event rates in the indicated population expected with standard of care; perform statistical risk assessments; use historical clinical trial data and other data sources to contextualize potential safety issues for new medications; support benefit-risk assessments throughout the product lifecycle; design and conduct post-authorization safety activities including rapid analytics for signal strengthening and formal required/committed evaluation studies as part of Pharmacovigilance and Risk Management Plans.
• Be involved in supporting efforts for the Office of the Chief Medical Officer and cross-sector collaborations as prioritized.
• Promote the use of standardized tools to support real world evidence generation across functions utilizing RWE as part of the Integrated Evidence Generation Plan.
• Keep up to date with changes in the external environment including working through professional society and public-private consortia to advocate as a subject matter expert regarding RWE guidance/framework for regulatory decision making.

Qualifications:

• PhD in Epidemiology or a closely related field OR MD with training and degree in Epidemiology or a closely related field OR Masters degree with at least 6 years of hands-on experience is required.
• At least 5 years of Epidemiology research experience is required.
• Understanding and the ability to apply and interpret quantitative methods is required.
• Experience writing observational study protocols proposals and proposal requests particularly the methods sections is required.
• Experience working with large administrative or medical records databases is required.
• Background in the epidemiologic landscape of oncology including related conditions and therapies is required.
• A track record of authoring scientific communications (peer-reviewed publications poster or oral presentations at conferences technical reports) is required.
• Experience working with health authorities is preferred.
• Product development experience in the pharmaceutical industry is preferred.
• Experience working in a global cross-functional team environment is preferred.
• The preferred location for this position is either Raritan NJ Titusville NJ or Horsham PA. Consideration may also be given for Spring House PA or Cambridge MA. (No fully remote option.)

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 internal employees contact AskGS to be directed to your accommodation resource.

The anticipated base pay range for this position is $164000 to $282900. 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 corporations performance over a calendar/performance year. Bonuses are awarded at the Companys discretion on an individual basis. 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 Companys consolidated retirement plan (pension) and savings plan (401(k)).

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
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. 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.

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