Associate Principal Scientist,Outcomes Research,HIV Job Rahway area,New Jersey USA,Research/Development

Job Description

The Associate Principal Scientist/Associate Director, Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research.
Under the guidance of a senior leader, this position has primary responsibility for planning/managing real-world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, health technology assessment /reimbursement agencies, and health systems globally.
Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, health‑care resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta‑analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy dossiers for U.S. payers, and Global Value Dossiers for use by local subsidiaries in their health technology assessment submissions.

The incumbent is expected to work cross‑functionally with clinical development, medical affairs, biostatistics, market access, commercial and country affiliates. The incumbent may supervise external vendors or partners to execute these activities. The incumbent may have direct interactions with health technology assessment agencies, reimbursement decision makers, or national immunization technical advisory groups.

Role Summary

The Associate Principal Scientist/Associate Director, Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research.
Under the guidance of a senior leader, this position has primary responsibility for planning/managing real-world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, health technology assessment /reimbursement agencies, and health systems globally.
Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, health‑care resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta‑analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy dossiers for U.S. payers, and Global Value Dossiers for use by local subsidiaries in their health technology assessment submissions.

The incumbent is expected to work cross‑functionally with clinical development, medical affairs, biostatistics, market access, commercial and country affiliates. The incumbent may supervise external vendors or partners to execute these activities. The incumbent may have direct interactions with health technology assessment agencies, reimbursement decision makers, or national immunization technical advisory groups.

Responsibilities And Primary Activities

Helps achieve / sustain reimbursement and market access for the program and indications under their responsibility.
Critically assesses drivers and barriers to reimbursement and market access and provides input into clinical, regulatory, payer/access, marketing and evidence-generation strategy and programs.
In collaboration with internal teams and external partners, designs studies; authors study protocols; and develops measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications.
Responsible for study‑related…

Associate Principal Scientist, Outcomes Research, HIV