Associate – HEVA (Evidence Synthesis)

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Skills you'll use

What you'll do

• The overall purpose and main responsibilities are listed below:
• Assist HEVA team in assigned therapy area portfolio to plan and generate robust health economics and value based evidence to maximize the value propositions from both a global and US perspective working within the Market Access tripod
• Contribute to the execution of quality research projects, economic models, trial design recommendations and other activities in support of programs/products
• Seek opportunities to innovate HEVA value identification, evidence generation and dissemination process/plan to increase the relevance and impact of HEVA evidence to ensure reimbursement decisions optimal access
• Develop and maintain TA expertise
• People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEVA teams across various time zones
• Performance: (1) Contribute in the HEVA evidence generation plan: Support activities for research plan for pre-launch, launch and post-launch evidence for investigational and marketed drugs; Evidence generation plan includes burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective, and prospective observational studies, economic evaluations, development and analysis of patient-reported outcomes; Provide support with individuals and institutions, which may serve as resources for evidence generation purpose, etc. (2) Support execution of approved HEVA study(s) and manage ongoing study(s) if required: Supports the manager/HEVA product lead to manage and execute research studies to support the clinical, economic and humanistic value of products; Studies include but are not limited to burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective and prospective observational studies, economic evaluations, and patient-reported outcomes (3) Support development of core value dossier (CVD) and AMCP dossiers and provide strategic direction
• Process: (1) Assist HEVA team in development of HEVA strategic evidence material (2) Contribute in development of core HEVA strategic evidence generation processes, templates, and products across the portfolio in accordance to the scientific and value messages aligned with CVD, the US AMCP dossier, and HEVA contributions as appropriate to other submissions (3) Maintain adherence to the evidence generation guidelines and other standards relevant to HEVA evidence generation processes
• Stakeholder: (1) Work with HEVA, RWE, Clinical, Medical Affairs, Marketing, External Affairs and Market Access global or local teams in regions/areas to identify evidence generation and dissemination needs and assist in developing assigned deliverables (2) Assist HEVA team to prepare relevant & customized deliverables for these Teams

Who can apply

• · Experience: 3+ years of experience in HEOR for the pharmaceuticals industry, CRO consultancy or academia.
• · Soft and technical skills: Stakeholder management; writing/communication skills; external engagement and ability to work independently and within a team environment
• Strong analytical skills to translate clinical and economic information and messages into payer evidence strategies
• · Education: Advanced degree in life sciences/pharmacy/similar discipline or medical degree
• · Languages: Excellent knowledge of English language (spoken and written)

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