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Associate Director, Oncology Epidemiology

Remote / Online - Candidates ideally in
Benton, Saline County, Arkansas, 72158, USA
Listing for: Oncology Voice Network
Full Time, Remote/Work from Home position
Listed on 2026-07-23
Job specializations:
  • Research/Development
    Research Scientist, Clinical Research, Infectious Disease/ Epidemiology
Salary/Wage Range or Industry Benchmark: 137000 - 235750 USD Yearly USD 137000.00 235750.00 YEAR
Job Description & How to Apply Below
Position: Associate Director, Oncology Epidemiology - Full-time

Associate Director, Oncology Epidemiology

We are searching for the best talent for the role of Associate Director, Oncology Epidemiology. We have a preference for this position to be located in either Raritan, NJ or Horsham, PA. Remote work options in the US may be considered on a case‑by‑case basis if approved by the Company. The Associate Director, Oncology Epidemiology role is accountable for working independently and will also function under the supervision of more senior members of the department.

Job

Details
  • Job Function:
    Data Analytics & Computational Sciences
  • Job Sub‑Function:
    Epidemiology
  • Job Category:
    People Leader
  • Location:

    Horsham, Pennsylvania;
    Raritan, New Jersey;
    Remote in the United States considered
  • Employment Type:

    Full‑time
  • Posting Date:
    Jul 18, 2026
Primary Responsibilities
  • Assist with identifying research study needs, drafting proposals and protocols, and contributing to epidemiology strategy and study conduct across the clinical development program.
  • May conduct fit‑for‑purpose database and study feasibility assessments and execute analyses across the product cycle.
  • Conduct literature reviews and synthesis; provide assistance to clinical teams with study design; and identify and evaluate data resources to meet therapeutic needs.
  • Work closely with colleagues in the Observational Health Data Analytics group when defining research questions, developing epidemiological protocols, and implementing solutions.
  • Provide epidemiological and/or statistical consulting, education and support to product teams, and disseminate technical information through technical reports, presentations, and publication in peer‑reviewed literature, as agreed by the team.
  • Research natural history of diseases, both within and outside of existing electronic databases, to understand the inherent risks associated with the indication; statistical risk assessment; using historical clinical trial data and other observational databases to develop an understanding of potential safety issues for new medications and indications, based on experience with related compounds.
  • May work in cross‑departmental/sector committees, and/or other efforts supporting J&J Innovative Medicine.
  • Keep up to date with the FDA and other regulatory agencies regarding regulatory requirements for Post‑Approval Authorization Studies and Risk Management plans and the development of formal guidance for use of RWE 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 Master’s degree with at least 4 years of hands‑on experience is required.
  • At least 3 years of epidemiology research experience is required.
  • Must have an understanding and the ability to interpret quantitative methods.
  • Experience with writing observational study protocols, proposals, and/or proposal requests, particularly the methods sections, 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 large administrative or medical records databases is preferred.
  • Applied pharmacoepidemiology research is preferred.
  • Background in epidemiologic material on specific diseases, conditions, or therapies particularly relating to the oncology therapeutic area is preferred.
  • Experience working with health authorities is preferred.
  • Phase III/IV medicine development experience is preferred.
  • Experience working in a global environment is preferred.
Equal Opportunity

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…

Position Requirements
10+ Years work experience
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