Researching analyst

JSR Tech Consulting; United States; On-site; USD 110,000 - 170,000; Full time

Job summary

The Life Sciences Organization seeks a seasoned HEOR/RWE expert for a multi-year project. Ideal candidates hold a PharmD from a U.S. institution or a PhD with pharmacotherapy expertise and 2–3 years in RWE/HEOR.

You will design RWE studies, conduct literature reviews, manage data coding, and contribute to regulatory and market access insights across the drug lifecycle. Proficiency with Excel, data tools, and project management is essential.

Qualifications

• PharmD from a U.S. institution or PhD with pharmacotherapy concepts.
• 2–3 years of RWE experience or a related Master’s in HEOR, epidemiology, biostatistics, or public health.
• 1–2 years of pharmaceutical or CRO industry experience.
• RWE study design and protocol development experience.
• Strong literature review and evidence synthesis capabilities.
• Knowledge of healthcare coding systems; experience with code lists (NDC, ICD-10-CM, etc.).
• Familiarity with FDA approvals, indications, LOE, biosimilars, and generics.
• Proficiency in Excel, Word, PowerPoint.
• Attention to detail and clear communication of complex information.
• Project management skills for timelines and multiple projects.

Skills

RWE study design

Literature review

Coding systems knowledge

Product lifecycle knowledge

MS Office

Attention to detail

Project management

SQL/R/Python/SAS

Real-world data sources

Education

PharmD (US)

Master’s in HEOR/related field

Tools

RED BOOK

AnalySource

Medi-Span

Job description

Our client, a global Life Sciences organization, is seeking a candidate for a multi-year project.

Qualifications

Doctor of Pharmacy (A PharmD 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 and extensive experience developing and validating code lists (e.g., NDC, GPI, HCPCS, ICD-9-CM, and ICD-10-CM codes); experience with RED BOOK or AnalySource, and Medi-Span
• Strong k nowledge 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)