Global Scientific Content Manager HEVA and PDMD

Job title : Global Scientific Content Manager - HEVA and PDMD Hiring Manager: Head/Group Lead/Team Lead – Scientific Writing Location: Hyderabad % of travel expected: As per business need Job type: Permanent and Full time About the job Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization 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, HEVA (including Patient-Driven Medicines Development [PDMD]), and Commercial organizations in Sanofi, Globally. Main responsibilities: The overall purpose and main responsibilities are listed below: Scientific Engagement Support the development of the integrated strategy for scientific expert engagement; scientific congress, scientific events and medical education; scientific dissemination; and multichannel engagement (in collaboration with global and local colleagues covering this area) for the assigned therapeutic area/products. Ensure timely execution of the scientific dissemination, scientific expert engagement, and medical multichannel engagement plans for global and countries. Support the development of engagement plans by identifying new multi-channel customer facing/engagement initiatives that will enhance the customer experience for scientific and medical learning and improvement of patient care, incorporating patient-centric perspectives and patient-reported outcomes (PROs). Closely track emerging and evolving digital technologies across industries, with a focus on healthcare & pharmaceutical industries, leveraging proof of concept to test ideas and channels. Support the development and expansion of a network of experts in the disease areas of responsibility through expert/KOL mapping activities that includes identification, profiling, and segmentation of international experts including emerging leaders and rising stars. Work closely with geographic segments/regions and countries to harmonize expert mapping activities and engagement plans. Establish and maintain professional and collaborative relationships with internal stakeholders, KOLs, scientific and academic societies, patient association and advocacy groups, medical communication and strategy companies involved. Attend the medical meetings, advisory boards, outreach meetings at key institutions, and interact with key experts, academic societies, and advocacy groups. Support the management and oversight of Scientific Congresses / Events, Donations and Other Contributions, advisory board planning & organization, compliance & transparency requirements. Scientific Publications and Medical Communications Support the development and oversight of strategic scientific publication plans and execution of operational and tactical activities within the overall medical communication platforms for assigned products/disease areas of responsibility (including HEVA and PDMD research outputs such as patient-reported outcomes, qualitative patient studies, and real-world evidence). Support the planning and proposal of content deliverables aligned with the strategic imperatives supporting the assigned products/disease areas. This includes reviewing and identifying relevant clinical findings, disease burden, unmet needs, patient-reported outcomes, and then proposing the development of corresponding compelling content. Serve as a key scientific reviewer, performing thorough quality control, scientific/clinical accuracy checks, and peer review of all draft manuscripts, abstracts, posters, slide decks, and value communication documents prior to stakeholder/author circulation. Ensuring timely delivery of high-quality, fair-balanced, scientifically/clinically accurate medical communications resources (including but not limited to proactive/reactive manuscript and poster/oral presentation slide decks, scientific platforms, lexicons, FAQs/trainings, symposia materials, medical booth materials, webinars, congress related microsites), scientific publication projects (including but not limited to manuscripts, abstracts, posters, and oral presentations, and enhanced content such as video, infographic, PLS, and podcast), internal communication and education resources (including but not limited to publication alerts, yammer communication of publications and congress events, pre-congress training slide deck, congress newsletters and reports), and integration of digital enhancements in medical publications in accordance with established timelines, compliance guidelines/policies, and budgets, in collaboration with the scientific writers and occasionally external agencies. Providing oversight, quality control, scientific review, and project management, for scientific publication and medical communication projects, ensuring accuracy, quality, and adherence to project timelines. Providing direction, constructive editorial review, and guidance to internal and external scientific writers, stakeholders, and regional partners regarding assigned projects, to ensure high-quality alignment with medical/scientific objectives, content development and dissemination processes, and adherence to Standard Operating Procedures. Maintain knowledge of international requirements and guidance associated with scientific publications/medical communications and their associated tools (iEnvision, PromoMats etc.). Ensure global and local teams are informed about the availability and relevance of developed content assets. Analyse regularly content usage data to evolve medical content development. Additional Maintain a keen understanding of the key stakeholder and patient community needs. Incorporate customer-specific insights, gaps, patient burden/lived experience insights, and needs in crafting strategies supporting overall medical/business priorities. Support the adoption of innovative content formats and processes, staying current with internal content evolution and industry trends. Ensure designated activities are appropriately executed, adherent to corporate SOPs and policies, and consistent with relevant external scientific, legal, and regulatory standards. Collaborate closely with colleagues as well as cross-functionally within a matrix organization (including HEVA, Global Medical Affairs, and Clinical teams) to ensure that information and knowledge transfer is conducted with internal and external stakeholders. Maintain transparency with peers and colleagues across the organization, to produce aligned strategy and tactics, while promoting synergy and avoiding duplication of effort. People: (1) Maintain effective relationship with the stakeholders (medical affairs, HEVA/PDMD, marketing, communications, regulatory affairs, medical scientific community etc.) within the allocated Global Business Unit and product – with an end objective to disseminate education and communication content as per requirement; (2) Interact effectively with internal teams and health care professionals on developed content; and (3) Constantly guide mentor, and peer-review the work of scientific writers in developing content and sharing expertise Performance: (1) Oversee the development, scientific review, quality assuran