Johnson & Johnson

Associate Director, Benefit Risk, Patient Preference

Johnson & Johnson

full-time

Posted on:

Location Type: Hybrid

Location: TitusvilleMassachusettsNew JerseyUnited States

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Salary

💰 $137,000 - $235,750 per year

Job Level

About the role

  • Leading structured benefit-risk assessments and patient preference studies including: Guiding clinical teams in benefit-risk assessment of products in development
  • Leading preference studies to support products in development, including designing preference studies for internal advisory boards
  • Applying structured patient preference, benefit-risk and decision analysis methods throughout the development lifecycle
  • Contributing as an author to internal and regulatory documents (e.g. statistical analysis plans, submission documents)
  • Serving as an internal subject matter expert on these topics
  • Keeping up to date with guidance and policy produced by regulatory agencies and other critical organizations regarding methodologies for benefit-risk assessment, patient preference studies and patient-focused drug development.
  • Lead benefit-risk and preference studies for development strategy, dose selection, clinical trials, regulatory documents, health authority advisory committee meetings, safety decisions, treatment access and providing guidance on use of real-world evidence in benefit-risk assessment.
  • Assist with internal benefit-risk process development and training, developing novel means to communicate and display preference and benefit-risk information, participating in external benefit-risk methodology and policy activities, authoring publications on their research and presenting at internal/external meetings.
  • Work closely with members of the Global Epidemiology, Clinical and Global Medical Safety departments and collaborate with colleagues in cross-functional teams in performing these responsibilities.

Requirements

  • Master’s degree in Decision Sciences, Health Economics, Epidemiology, Biostatistics, Public Health, or a related scientific discipline required; PhD or MD strongly preferred.
  • A minimum of 5 years (3 year for PhD or MD) of hands-on experience in patient preference, benefit-risk, applied statistical or epidemiologic research
  • Knowledge of current academic/regulatory/industry trends in structured benefit-risk, preference studies and patient-focused drug development.
  • Experience using structured benefit-risk frameworks (e.g., FDA benefit-risk framework, BRAT, PrOACT-URL) and/or experience with patient preference studies (e.g., discrete choice experiments, best-worst scaling, threshold technique).
  • Experience leading projects with multi-stakeholder teams (e.g., clinical, statistics, regulatory) on technical projects.
  • Experience presenting technical topics to clinical/medical audiences.
  • Excellent communication (verbal and written) and interpersonal skills.
  • The ability to collaborate with all levels in a cross-functional team environment.
  • Strong problem-solving skills.
  • Strong self-management skills with a focus on timely completion of competing deliverables.
Benefits
  • 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)).
  • 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 period
  • Volunteer Leave – 32 hours per calendar year
  • Military Spouse Time-Off – 80 hours per calendar year

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
benefit-risk assessmentpatient preference studiesdecision analysis methodsstatistical analysisreal-world evidencestructured benefit-risk frameworksdiscrete choice experimentsbest-worst scalingthreshold techniqueapplied statistical research
Soft skills
communication skillsinterpersonal skillscollaborationproblem-solvingself-managementleadershipproject managementpresentation skillsteamworkadaptability
Certifications
Master’s degree in Decision SciencesMaster’s degree in Health EconomicsMaster’s degree in EpidemiologyMaster’s degree in BiostatisticsMaster’s degree in Public HealthPhDMD