About the Company: Sanofi Business Operations (SBO) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines,CHC,CMO, and R&D, Data & Digital functions​. SBO strives to be a strategic and functional partner for tactical deliveries to Medical, Health Economics and Value Assessment (HEVA), and Commercial organizations​ in Sanofi, globally.

About the Role: Job title: Associate – Evidence SynthesisHiring Manager: Head/Group Lead//Team LeadLocation: Hyderabad% of travel expected: Travel required as per business needJob type: Permanent and Full timeAbout the jobOur Team:Sanofi Business Operations (SBO) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions​. SBO strives to be a strategic and functional partner for tactical deliveries to Medical, Health Economics and Value Assessment (HEVA), and Commercial organizations​ in Sanofi, globally.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 marketsSeek 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 accessDevelop and maintain therapeutic area (TA) expertisePeople: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEVA/Medical teams across various time zonesPerformance: (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 directionProcess: (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 processesStakeholder: (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 TeamsAbout youExperience: 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 environmentTechnical skills: Strong analytical skills to translate clinical and economic information and messages into payer evidence strategiesEducation: Advanced degree in life sciences/pharmacy/similar discipline or medical degreeLanguages: Excellent knowledge of English language (spoken and written)Pursue progress, discover extraordinaryBetter is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Key Responsibilities: 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 marketsSeek 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 accessDevelop and maintain therapeutic area (TA) expertisePeople: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEVA/Medical teams across various time zonesPerformance: (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 directionProcess: (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 processesStakeholder: (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