Our client is looking to fill the role of HEOR Consultant. This position will be fully remote. This position serves as the lead for HTA launch readiness projects for Nephrology products. Supports under the Director, Health Outcomes this individual will develop elements of a dossier, Systematic lit reviews and HE models, used to deliver on evidence strategy across product life cycle for HTA/payer needs.
Responsibilities:
High quality health economics and payer evidence input into pharmaceutical development projects, payer evidence strategy and plans
Participate in external health economics and payer evidence departmental activities via technical presentations, publication development, and other activities
This role is part of a global cross-functional team and interacts with Global Clinical Development, Clinical Management, Regulatory Affairs, Biostatistics, Global Medical Affairs, Commercial, Market Access, Government Affairs, and other colleagues to stay abreast of clinical development program needs for value differentiation in alignment with the target product profile across the product lifecycle.
High quality health economics and payer evidence input into pharmaceutical development projects, and payer evidence plans
Deliver clear, customer-focused and robust Global Reimbursement Dossiers (GRDs)
Advocate and champion the need for scientifically sound trial and non-trial data (including RWE, economic modelling, meta-analyses, observational studies, and PRO approaches
Communicate study plans, study methods, and results to internal teams
Present research findings at scientific congresses and/or via manuscripts
Maintain awareness, education on and implementation of HEOR methods (qualitative, quantitative, interventional, and non-interventional), tools, and data sources to ensure study methods represent current state of science, as well as assessment and interpretation of relevant literature, scientific dissemination in line with internal communication
Manage budget resources allocated to assigned projects
Willingness to travel to offsite events including conferences and stakeholder meetings.
Required Qualifications:
Graduate degree in biomedical science, business, quantitative disciplines or economics (outcomes research, health services research, epidemiology, public health, community health, or related fields).
Formal post-graduate degree (or equivalent applied work) in health economics or a related quantitative discipline, as well as related work experience.
At least 5+ years professional experience in evidence generation in a pharmaceutical or consulting role.
Excellent knowledge of clinical development and research study designs and interpretation.
Good understanding of qualitative and quantitative approaches.
Comprehensive understanding of the pharmaceutical industry and regulatory requirements from a global perspective and product development processes at all life cycle stages.
Good working knowledge of international healthcare systems and their changing needs for HTA submission purposes.
Experience with vendor and external contractor oversight.
Project Management experience.
If you meet the required qualifications and are interested in this role, please apply today.
Clinical Resource Network Distinction
CRN, a division of Solomon Page, offers a comprehensive benefits program for hourly employees. We pride ourselves on offering medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits to our employees, including consultants - which sets us apart in the industries we serve.
About CRN
Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies. Focused on forming long-term relationships, services encompass contract staffing, project staffing, consultative services, and full-time placements. For more information, visit https://www.solomonpage.com/crn and connect with us on Facebook and LinkedIn.