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JT

Researching analyst

JSR Tech Consulting
  • Location not stated
  • Remote
  • 6 hours ago
  • PharmD
  • HCPCS
  • ICD-10-CM
  • Excel
  • PowerPoint
  • 340B
  • CMS
  • SQL
  • Python
  • SAS
  • EHR
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Our client, a global Life Sciences organization, is seeking a candidate for a multi-year project.

Qualifications
 
Doctor of Pharmacy(APharmD from a U.S.institution or a Ph.D  with a strong understanding of pharmacotherapy and clinical concepts comparable to PharmD-level training) and (2-3 years of experience in RWE or a master's degree in Health Economics and Outcomes Research (HEOR), Epidemiology, Biostatistics, Public Health, or a related field).
  • At least 1-2 years of pharmaceutical or CRO industry experience.
  • RWE study experience, including study design and protocol development, such as defining study populations, inclusion/exclusion criteria, index dates, baseline and follow-up periods, exposures/interventions, and outcomes.
  • Strong literature review and evidence synthesis skills, including the ability to critically review and interpret clinical trials and treatment guidelines
  • Strong knowledge of healthcare coding systems andextensiveexperience developing and validating code lists (e.g., NDC, GPI, HCPCS, ICD-9-CM, and ICD-10-CM codes); experience with RED BOOK orAnalySource, and Medi-Span
  • Strong knowledge of pharmaceutical product characteristics and lifecycle events, including FDA approvals, indications, label expansions, orphan drug designations, loss of exclusivity (LOE), biosimilars, and generic competition
  • Proficiency in Microsoft Excel, Word, and PowerPoint
  • Attention to detail, with the ability to organize, synthesize, and communicate large volumes of complex information
  • Strong work ethic and learning agility
  • Project management experience, including the ability to manage timelines, deliverables, and multiple concurrent projects
 
Preferred Experience and Skills
  • Experience with health economic modeling (e.g., budget impact models and cost-effectiveness analyses)
  • Understanding of U.S. healthcare policy and reimbursement, including the Inflation Reduction Act (IRA), the 340B Drug Pricing Program, Medicare policy, and related pharmaceutical market access considerations
  • Experience reviewing and interpreting Centers for Medicare & Medicaid Services (CMS) guidance, policy documents, and healthcare regulations
  • Experience conducting systematic literature reviews
  • Programming and data analytics experience using SQL, R, Python, SAS, etc.
  • Strong knowledge of real-world data sources (e.g., administrative claims, electronic health records [EHRs], and registries)
  #LI-TI1

Researching analyst · JSR Tech Consulting

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