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Associate Director, Global Market Access Analytics, RWE
Job in
Raritan, Somerset County, New Jersey, 08869, USA
Listed on 2026-07-13
Listing for:
Jobtailor
Full Time
position Listed on 2026-07-13
Job specializations:
-
Research/Development
Data Scientist, Research Scientist, Research Analyst
Job Description & How to Apply Below
Responsibilities
- Design and conduct analyses that align to payer (e.g. CDA, NICE, HAS) and regulatory evidentiary requirements and fully leverage available data sources.
- Lead the design and execution of indirect treatment comparisons (e.g., MAIC, STC, NMA, ML-NMR), observational studies, and comparative effectiveness analyses.
- Provide expert guidance on statistical methodologies and programming approaches to address key research questions in collaboration with therapeutic area experts.
- Lead end-to-end delivery of evidence-generation work streams, including systematic literature reviews, feasibility assessments, protocol development, statistical analysis plans, and technical reports/publications.
- Apply advanced statistical methods such as regression modeling, mixed-effects models, survival analysis, propensity score methods, and non-parametric techniques in accordance with study protocols.
- Partner across internal functions (e.g., Global Market Access, R&D, Medical Affairs, Health Economics Modeling, Epidemiology) to develop evidence generation strategies that optimize HTA outcomes.
- Engage and collaborate with external partners, providing scientific and technical input to support joint research initiatives.
- Advanced degree (Master’s or higher) in a relevant field such as biostatistics, mathematics, computational sciences, economics, public health, health administration, or operations research.
- Minimum of 6+ years of relevant experience (or 4+ years with a doctoral degree) in pharmaceutical, biotech, or consulting environments.
- Demonstrated proficiency in statistical programming, including R, SAS, and other relevant tools.
- Ability to design and apply statistical methods for comparative effectiveness research, including indirect treatment comparisons and secondary data analyses.
- Hands‑on experience analyzing diverse data sources, including clinical trial data, data extracted in systematic literature reviews, administrative claims, electronic health records, and clinical registries.
- Strong organizational skills and ability to manage multiple priorities in a fast‑paced environment, with a track record of meeting deadlines.
- Effective project management capabilities, including planning, prioritization, and execution across concurrent work streams.
- Excellent written and verbal communication skills, with the ability to convey complex technical information to diverse audiences.
- statistical programming
- regression modeling
- mixed‑effects models
- survival analysis
- propensity score methods
- non‑parametric techniques
- comparative effectiveness research
- indirect treatment comparisons
- data analysis
- systematic literature reviews
- organizational skills
- project management
- communication skills
- collaboration
- ability to manage multiple priorities
- execution capabilities
- planning
- prioritization
- track record of meeting deadlines
- ability to convey complex information
Position Requirements
10+ Years
work experience
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