Director of Oncology Epidemiology at Johnson & Johnson managing epidemiology projects and real-world evidence research. Overseeing analyses, leading projects, and collaborating across functions for innovative medicine.
Responsibilities
accountable for working independently while functioning under the supervision of more senior members of Global Epidemiology
responsible for oversight of various projects and initiatives in areas of epidemiology and real-world evidence research
leading research projects, drafting protocols and statistical analysis plans
overseeing the analysis of real-world data and dissemination of scientific information through technical reports, presentations, and publications
Identify research study needs, drafting proposals and protocols, contributing to real-world evidence strategy and study conduct
Work closely in collaboration with colleagues in the Epidemiology group when defining research questions
Participate in various multi-disciplinary matrix teams to address issues raised by product teams/regulatory agencies
Provide epidemiological and/or statistical consulting and support to compound/product teams
Keep up to date with changes in the external environment regarding RWE guidance/framework for regulatory decision making
Requirements
PhD in Epidemiology or a closely related field OR MD with training and degree in Epidemiology or a closely related field OR Master’s 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.
Benefits
medical, dental, vision, life insurance
short- and long-term disability
business accident insurance
group legal insurance
consolidated retirement plan (pension)
savings plan (401(k))
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
Work, Personal and Family Time - up to 40 hours per calendar year
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