job title: Associate evidence synthesis(sanofi)

Roles and Responsibilities

Main responsibilities:

The overall purpose and main responsibilities are listed below:

• Contribute at different levels in execution of assigned Evidence Synthesis projects (including but not limited to search strategy development, screening, data extraction) to generate robust evidence to maximize the value propositions in support of programs/products for Global/Local markets

• Seek opportunities to innovate HEVA/Medical value identification, evidence generation and dissemination process/plan to increase the relevance and impact of HEVA/Medical evidence to ensure reimbursement decisions and optimal access

• Develop and maintain therapeutic area (TA) expertise

• People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEVA/Medical teams across various time zones

• Performance: (1) Contribute at different levels in execution of assigned Evidence Synthesis projects (including but not limited to search strategy development, screening, data extraction): 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/Medical study(s) and manage ongoing study(s) if required: Supports the HEVA/Medical product lead to manage and execute research studies to support the clinical, economic and humanistic value of products (3) Support development of core value dossier (CVD) and Academy of Managed Care Pharmacy (AMCP) dossiers and provide strategic direction

• Process: (1) Assist HEVA/Medical team in development of strategic evidence material (2) Contribute in development of core strategic evidence generation processes, templates, and products across the portfolio in accordance to the scientific and value messages aligned with CVD, AMCP dossier, and as appropriate to other submissions (3) Maintain adherence to the evidence generation guidelines and other standards relevant to 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/Medical team to prepare relevant & customized deliverables for these Teams

About you

• Experience: 3+ years of experience in Health Economics and Outcomes Research (HEOR) for the pharmaceuticals industry, CRO consultancy or academia.

• Soft skills: Stakeholder management, writing/communication skills, external engagement and ability to work independently and within a team environment

• Technical skills: 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)