Head of Medical Information - Medical Affairs

2d2 days ago

Vor Bio

Boston, US · Full-time · $220,000 – $295,000

About this role

The Head of Medical Information will lead the function within Medical Affairs at Vor Bio. This senior leader builds and runs the MI function while preparing for the company’s first regulatory approval and commercial launch. The role is primarily US-focused with global responsibilities.

Day-to-day work centers on accurate and compliant responses to inquiries from HCPs, patients, and internal stakeholders. The leader serves as the primary point of accountability with compliance, quality, and safety & pharmacovigilance teams. All activities align with regulatory standards and company policies.

The position requires close partnership with Pharmacovigilance, Regulatory Affairs, Commercial, and IT. The MI lead establishes operational infrastructure including inbound channels, escalation pathways, and documentation requirements ahead of US launch. Cross-functional launch readiness governance is a core responsibility.

Team members contribute directly to a medicine with best-in-disease Phase 3 results in myasthenia gravis and expansion into multiple autoimmune diseases. The role offers opportunities to grow a career in science, clinical development, and commercial strategy within a rapidly scaling company.

Requirements

Experience leading a medical information function within Medical Affairs in the pharmaceutical industry.
Proven ability to build MI operational infrastructure and governance documents prior to product launch.
Strong knowledge of regulatory requirements for medical information responses and pharmacovigilance integration.
Experience developing and maintaining Standard Response Documents and content governance processes.
Demonstrated success implementing medical information systems and ensuring data protection compliance.
Track record of leading cross-functional collaboration with Pharmacovigilance, Regulatory Affairs, and Commercial teams.

Responsibilities

Lead the end-to-end buildout of the MI function, covering team, technology, content, SOPs, and vendor ecosystem.
Develop and execute the global MI strategy aligned with company objectives and regulatory standards.
Establish MI operational infrastructure, including inbound channels, escalation pathways, response turnaround standards, and documentation requirements.
Ensure global compliance with regulatory requirements and integration with the pharmacovigilance safety database and medical CRM.
Develop, implement, and maintain all MI governance documents including SOPs, policies, and working instructions.
Oversee development of the Standard Response Documents library and ensure scientifically accurate, balanced, and up-to-date SRDs and FAQs.
Lead, mentor, and develop a high-performing MI team while fostering a culture of scientific excellence and compliance rigor.
Serve as the primary MI representative in cross-functional launch readiness governance and provide regular performance reporting.

Benefits

Contribute directly to a medicine with best-in-disease Phase 3 results in myasthenia gravis.
Be part of a rapidly scaling company with opportunities to grow your career in science and clinical development.
Work on a platform with potential beyond one indication across lupus, IgA nephropathy, and Sjögren’s syndrome.
Join a culture where every voice is heard and shared mission unites teams across functions.