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Rilzabrutinib Medical Launch Lead

10+ years
USD 202,500.00 - 337,500.00
10 Oct. 27, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

๐ŸŒ Job Title: Rilzabrutinib Medical Launch Lead

๐Ÿ“ Location: Cambridge, Massachusetts, USA
๐Ÿข Department: Global Medical – Rare Diseases
๐Ÿ•’ Employment Type: Regular (Onsite)
๐Ÿ’ฐ Salary Range: USD 202,500 – 337,500
๐Ÿ‘ค Hiring Manager: Mario Aguiar
๐Ÿ“… Posted On: October 2, 2025
๐Ÿ“… Closing On: January 23, 2026


About the Role

The Rilzabrutinib Medical Launch Lead will play a critical role in the global medical launch strategy for Rilzabrutinib, a best-in-class treatment for Immune Thrombocytopenia (ITP) and Warm Autoimmune Hemolytic Anemia (wAIHA).

Reporting to the Global Head of Rare Launch and Pipeline Portfolio within the Global Medical Rare Disease Organization, this role is responsible for shaping and executing the global medical strategy, evidence generation, and stakeholder engagement activities that ensure successful launch and market introduction.

This position offers a high-impact opportunity to collaborate across multiple global teams, lead medical initiatives pre-launch, and contribute to advancing rare disease innovation within a trusted, patient-focused organization.


Main Responsibilities

๐Ÿ”น Strategic Medical Leadership

  • Develop and execute the Global Medical Strategy and action plan for Rilzabrutinib.

  • Serve as the Medical Representative within the Rilzabrutinib Global Development Team (GDT), ensuring cross-functional alignment and delivery of key milestones.

  • Collaborate closely with the Global Product Head (GPH) to lead all pre-launch medical activities.

๐Ÿ”น Evidence Generation & Clinical Strategy

  • Partner with the Medical Evidence Generation and Global Product Teams to design and implement the Evidence Generation Plan (EGP) supporting product development.

  • Lead the design of new clinical studies focused on clinically relevant and patient-centric outcomes.

  • Oversee the Global Labelling Process for all Rilzabrutinib indications.

๐Ÿ”น Launch Execution

  • Drive development and global implementation of the Managed Access Program (MAP) for Rilzabrutinib in ITP and wAIHA.

  • Define the Global Strategy for Clinical Insights, KOL Mapping, and Message Dissemination.

  • Ensure the medical readiness of global teams for Wave-1 regulatory submissions and approvals.

๐Ÿ”น Cross-Functional & Stakeholder Collaboration

  • Act as the key liaison between Global Development, Medical Affairs, Regulatory, Commercial, and Clinical Operations.

  • Provide medical expertise in high-stakes interactions with regulatory authorities, scientific leaders, and medical societies.

  • Support strategic planning, budget allocation, and resource optimization across medical initiatives.


About You

๐ŸŽ“ Qualifications

  • Medical Degree (MD) or PhD (preferred)

  • Expertise in Rare Hematologic Disorders or related therapeutic areas

๐Ÿ’ผ Experience

  • Minimum 10 years of experience in evidence generation, including clinical development and/or real-world evidence (RWE)

  • Recognized global or peer-level thought leader in area of expertise

  • Demonstrated success leading cross-functional teams and managing budgets

  • Proven ability to influence and lead in a matrixed, multicultural environment

๐Ÿ’ฌ Key Skills

  • Strong communication and public speaking skills

  • Strategic mindset with ability to connect scientific insight to business impact

  • Skilled in stakeholder management and medical governance

  • Adept at navigating complex regulatory landscapes


Why Join Sanofi

  • Be part of a legacy — over 30 years of leadership in Rare Diseases and innovation for unmet medical needs.

  • Work with purpose — contribute to advancing treatment for patients with serious rare disorders.

  • Grow globally — pursue career development opportunities within a dynamic, science-driven organization.

  • Enjoy exceptional benefits:

    • Competitive compensation and performance-based rewards

    • Comprehensive healthcare and wellness programs

    • 14 weeks of gender-neutral parental leave

    • Access to global mobility and continuous learning programs


Equal Opportunity Statement

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action Employers, committed to building a culturally diverse workforce.
All qualified applicants will be considered without regard to race, color, religion, gender, national origin, age, sexual orientation, disability, veteran status, or any protected characteristic under applicable law.


๐Ÿ“Ž Additional Details

Tags: #GD-SG #LI-GZ #LI-Onsite #VHD
Compensation: Based on demonstrated experience and eligibility for employee benefit programs.

๐Ÿ”— Apply Now: Sanofi Careers Portal
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