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Form of workJob Description
Position Details:
Our client, a world-leading Pharmaceutical Company in New York, NY is currently looking for a Research Associate / Public Health HEOR / HYBRID WORK to join their expanding team.
Job Title: Research Associate / Public Health HEOR / HYBRID WORK
Duration: 12 months contract, extendable up to 36 months
Location: New York, NY
Hybrid work: 2-3 days/Onsite
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Provide study and operational support to HEOR V&E with a focus on IDM.
Assist study lead(s) in the end-to-end process of an HEOR project or ancillary activities.
This includes preparing study information and materials (eg, study protocols, project memo, manuscript outlines) in accordance with corporate policies and requirements, vendor management, interactions with external thought leaders, development of presentations/reports & publication support, identification of publications, informal literature searches.
Responsibilities
Under the guidance of a senior leader, a Research Associate has primary responsibility for planning/managing real world and economic evidence activities for in-line products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally
Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling
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 (HTA) agencies, reimbursement decision makers, or national immunization technical advisory groups
Participate in value evidence teams and serves as outcomes research representative on cross-functional regional and global teams
Critically assess drivers and barriers to reimbursement and market access, and provide input into clinical, regulatory, payer/access, marketing and evidence generation strategy and programs
In collaboration with internal teams and external partners, design studies, author study protocols, develop measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications
Responsible for study-related contracting, budgets, and vendor/partner management
Develop supplementary clinical data package in close partnership with markets and HTA statistics group for submission to HTA agencies
Support country affiliates to understand local evidence generation needs, adapt health economic evaluations, customize outcomes research documents, such as protocols and reimbursement dossiers, according to local requirements
Work closely with cross functional teams to effectively communicate outcomes research and health economic modelling data internally and to external customers
Maintain awareness of new scientific and methodological developments within therapeutic area
Present outcomes research data at national and international congresses and publish articles in scientific journals.
Skills:
Must have: highly detail-oriented, takes a structured and organized approach to work, excellent communication skills, has academic background and understanding of targeted and systematic literature reviews.
Nice to have: infectious disease experience (theory and/or practice), HEOR modelling expertise, practical experience with retrospective or prospective Outcomes Research studies.
Interview Process:
1:1 and potential panel interview.
Comments:
Hybrid - local to NYC HQ location.
Minimum Education:
Masters degree in relevant discipline (health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, pharmacy administration)
Experience in outcomes research, health economics, epidemiology, public health and related fields is required
Working experience in pharmaceutical industry is preferred.
Preferred: 1-3 years post degree
Our client, a world-leading Pharmaceutical Company in New York, NY is currently looking for a Research Associate / Public Health HEOR / HYBRID WORK to join their expanding team.
Job Title: Research Associate / Public Health HEOR / HYBRID WORK
Duration: 12 months contract, extendable up to 36 months
Location: New York, NY
Hybrid work: 2-3 days/Onsite
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Provide study and operational support to HEOR V&E with a focus on IDM.
Assist study lead(s) in the end-to-end process of an HEOR project or ancillary activities.
This includes preparing study information and materials (eg, study protocols, project memo, manuscript outlines) in accordance with corporate policies and requirements, vendor management, interactions with external thought leaders, development of presentations/reports & publication support, identification of publications, informal literature searches.
Responsibilities
Under the guidance of a senior leader, a Research Associate has primary responsibility for planning/managing real world and economic evidence activities for in-line products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally
Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling
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 (HTA) agencies, reimbursement decision makers, or national immunization technical advisory groups
Participate in value evidence teams and serves as outcomes research representative on cross-functional regional and global teams
Critically assess drivers and barriers to reimbursement and market access, and provide input into clinical, regulatory, payer/access, marketing and evidence generation strategy and programs
In collaboration with internal teams and external partners, design studies, author study protocols, develop measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications
Responsible for study-related contracting, budgets, and vendor/partner management
Develop supplementary clinical data package in close partnership with markets and HTA statistics group for submission to HTA agencies
Support country affiliates to understand local evidence generation needs, adapt health economic evaluations, customize outcomes research documents, such as protocols and reimbursement dossiers, according to local requirements
Work closely with cross functional teams to effectively communicate outcomes research and health economic modelling data internally and to external customers
Maintain awareness of new scientific and methodological developments within therapeutic area
Present outcomes research data at national and international congresses and publish articles in scientific journals.
Skills:
Must have: highly detail-oriented, takes a structured and organized approach to work, excellent communication skills, has academic background and understanding of targeted and systematic literature reviews.
Nice to have: infectious disease experience (theory and/or practice), HEOR modelling expertise, practical experience with retrospective or prospective Outcomes Research studies.
Interview Process:
1:1 and potential panel interview.
Comments:
Hybrid - local to NYC HQ location.
Minimum Education:
Masters degree in relevant discipline (health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, pharmacy administration)
Experience in outcomes research, health economics, epidemiology, public health and related fields is required
Working experience in pharmaceutical industry is preferred.
Preferred: 1-3 years post degree
