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    Sr. Associate – Heva (Evidence Synthesis)

    Sanofi
    2+ years
    Not Disclosed
    Hyderabad
    10 Nov. 7, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Sr. Associate – HEVA (Health Economics & Value Assessment)

    Location: Hyderabad, India
    Job Type: Full-Time, Permanent
    Travel: As per business need

    About Us

    Sanofi Global Hub in Hyderabad is a strategic internal resource organization that centralizes processes and activities to support Sanofi's global operations across various functions, including Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, and Data & Digital. Our team is committed to driving operational excellence and supporting Sanofi’s Medical, HEVA, and Commercial teams with impactful and tactical solutions globally.

    We are currently seeking a Sr. Associate – HEVA to join our dynamic team. In this role, you will support the generation of robust health economics and value-based evidence for the products in your assigned therapy area, working closely with Market Access and global HEVA teams to ensure optimal access and reimbursement decisions.

    Main Responsibilities

    As a Sr. Associate – HEVA, your core responsibilities will include the development, execution, and management of evidence generation strategies to demonstrate the clinical, economic, and humanistic value of Sanofi’s products.

    Evidence Generation & Strategic Planning

    • Support HEVA Evidence Plan: Assist in the development of comprehensive evidence generation plans for investigational and marketed drugs, covering pre-launch, launch, and post-launch phases. This includes managing studies such as burden of illness studies, epidemiology, meta-analysis, observational studies, economic evaluations, and patient-reported outcomes.
    • Study Execution & Support: Support the execution of approved HEVA studies and provide strategic oversight, ensuring the timely completion of studies related to clinical, economic, and humanistic product value.
    • Value Proposition Development: Collaborate with cross-functional teams to create Core Value Dossiers (CVD), AMCP dossiers, and other strategic evidence deliverables.

    Collaboration with Stakeholders

    • Cross-Functional Partnerships: Work closely with global and local teams including HEVA, RWE, Clinical, Medical Affairs, Marketing, External Affairs, and Market Access to ensure the identification and dissemination of evidence generation needs.
    • Stakeholder Engagement: Maintain effective relationships with key stakeholders and facilitate communication across various time zones and functions to ensure alignment on evidence generation plans and deliverables.

    Process Development & Compliance

    • HEVA Strategy & Templates: Assist the HEVA team in the development of evidence generation templates, materials, and processes, ensuring alignment with scientific, clinical, and value messages (e.g., CVD, AMCP dossiers).
    • Adherence to Guidelines: Ensure compliance with evidence generation guidelines and contribute to the development and maintenance of processes that ensure quality, integrity, and alignment with regulatory and scientific standards.

    About You

    To excel in this role, you will bring your expertise in Health Economics, Outcomes Research, and a solid understanding of the pharmaceutical industry, specifically within market access and reimbursement.

    Experience

    • 5+ years of experience in Health Economics & Outcomes Research (HEOR) within the pharmaceutical industry, CROs, or academia.
    • In-depth understanding of health economics, health technology assessment (HTA) reviews, and reimbursement processes.

    Skills & Competencies

    • Stakeholder Management: Proven ability to work with cross-functional teams and external stakeholders, building strong relationships to drive evidence generation goals.
    • Analytical & Communication Skills: Strong ability to translate clinical and economic data into clear payer evidence strategies, with excellent writing and communication skills.
    • Independence & Teamwork: Ability to work independently while also collaborating effectively within a team environment.
    • Technical Proficiency: Familiarity with HEOR methodologies, economic modeling, and epidemiological studies. Experience with value-based healthcare and payer strategies is a plus.

    Education

    • Advanced degree in Life Sciences, Pharmacy, or a similar discipline (Master's, PhD, or MD).

    Languages

    • Fluent in English (spoken and written).

    Why Choose Sanofi?

    At Sanofi, we are driven by the ambition to create better medications, improve patient outcomes, and foster scientific breakthroughs. By joining our team, you will have the opportunity to work alongside a diverse, inclusive team in a company committed to your growth and development.

    What We Offer:

    • Career Development: Opportunities for growth and career progression within an international organization.
    • Competitive Rewards: A well-crafted benefits package that recognizes your contribution.
    • Global Impact: The chance to contribute to groundbreaking healthcare innovations.

    Join us in our mission to pursue progress and discover extraordinary possibilities!

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