Vor Bio

Vor Bio

Head of Medical Information (Director/Senior Director) – Medical Affairs

Boston, MA · Director

Sponsorship not specifiedDetected 51 days ago
Data VisualizationProject ManagementStakeholder ManagementCRMExcelFDA RegulatoryPharmacovigilanceLeadershipCommunicationPublic SpeakingRegulatory Affairs

About the role

  • When you join Vor, you're not just working on a medicine.
  • Impact: Contribute directly to a medicine with best-in-disease Phase 3 results in myasthenia gravis and expansion into multiple autoimmune diseases.

Responsibilities

  • Lead the end-to-end buildout of the MI function, covering team, technology, content, SOPs, and vendor ecosystem, in alignment with the company's launch readiness timeline.
  • Develop and execute the global MI strategy aligned with company objectives and regulatory standards.
  • Develop, implement, and maintain all MI governance documents, including standard operating procedures (SOPs) and/or policies and/or working instructions (WIs).
  • Oversee development of Standard Response Documents (SRDs) library and content governance. Ensure the creation and maintenance of scientifically accurate, balanced, and up-to-date SRDs and and FAQs.
  • Drive the implementation and optimization of emerging technologies.
  • Lead, mentor, and develop a high-performing MI team. Foster a culture of scientific excellence, compliance rigor, and continuous improvement.
  • Establish and maintain the MI quality assurance program. Ensure MI data management practices comply with applicable data protection regulations.
  • Partner with cross-functional teams including Pharmacovigilance, Regulatory Affairs, Commercial, and IT to support product launches and lifecycle management.
  • Develop and track key performance indicators (KPIs) to monitor performance, quality, and compliance of MI services.
  • Scientific acumen sufficient to lead a global MI function in the autoimmune space

Requirements

  • Advanced degree (PhD, MD, PharmD, or equivalent) required.
  • Ability to operate effectively in a fast-paced, cross-functional environment.
  • Proficiency in scientific and clinical data review and interpretation.
  • Experience in immunology, auto-immune disease, and/or rare disease highly desirable.
  • We invite you to come as you are.

Nice to have

  • Boston, MA preferred
  • The scope of this role will be primarily US-focused but will also have global responsibilities.
  • Strong knowledge of applicable regulatory guidelines and standards.
  • Familiarity with ex-US regulatory frameworks and multi-country MI operations is preferred.

Skills

  • Deep knowledge of US regulatory frameworks governing medical information activities,
  • Excellent project management skills
  • Strong cross-functional leadership and stakeholder management skills
  • Excellent written and verbal scientific communication skills, with experience presenting to executive leadership teams.
  • Excellent organizational, managerial, and communication skills

Compensation

  • The salary range for the Hed of Medical Information at Director level is expected to be between $220,000 and $240,000 per year.

Benefits

  • Monitor and analyze trends in medical inquiries to inform internal stakeholders (e.g., Medical Affairs, Commercial, Pharmacovigilance, Regulatory).
  • Ensure global compliance with regulatory requirements and company policies and integration with the pharmacovigilance safety database, medical CRM, and document management system.
  • Education, Experience and

Company info

  • Be part of a rapidly scaling company with opportunities to grow your career in science, clinical development, commercial strategy, and beyond.
  • At Vor, we believe science can do more than manage symptoms.
  • By advancing telitacicept, a first- and potentially best-in-class dual BAFF/APRIL inhibitor, we are silencing upstream survival signals and stopping downstream autoimmune cascades.
  • Together, we are addressing disease at its root cause and rewriting what is possible for patients worldwide.
  • You're part of a mission to redefine the future of autoimmune care.
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