Our Team:
Sanofi Global Hub 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. MedHub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally.
Main responsibilities:
The overall purpose and main responsibilities are listed below:
- Assist at different levels in execution of assigned Evidence Synthesis projects (including but not limited to screening, data extraction, full-text downloading) to generate robust evidence to maximize the value propositions in support of programs/products for Global/Local markets
- Develop and maintain TA expertise
- Maintain adherence to the evidence generation guidelines and other standards relevant to HEVA evidence generation processes
- People: (1) Support the internal Sanofi Global Hub HEVA team in effective delivery of evidence generation projects
- Performance: (1) Assist at different levels in execution of assigned Evidence Synthesis projects (including but not limited to screening, data extraction, full-text downloading): 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 Sanofi Global Hub Evidence Generation team in 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
- Process: (1) Assist in development of HEVA strategic evidence material (2) Support 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) Assist HEVA team in their engagements 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
About you
- Experience: 1+ of experience in 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)
