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

Vor Bio•Boston, MA

1d•$220,000 - $295,000•Hybrid

About The Position

Join Vor Bio in tackling autoimmune disease at its root. Vor Bio is advancing telitacicept, a dual BAFF/APRIL inhibitor, to address disease at its root cause and rewrite what is possible for patients worldwide. This role is for a Head of Medical Information (MI) within Medical Affairs (MA), responsible for building and running the MI function in preparation for the company’s first regulatory approval and commercial launch. The role is primarily US-focused with global responsibilities. The MI lead will be accountable for leading the strategy and operations of the MI function, ensuring accurate, timely, and compliant responses to inquiries from healthcare professionals (HCPs), patients, and internal stakeholders, and will be the primary point of accountability with other functions across the company.

Requirements

Deep knowledge of US regulatory frameworks governing medical information activities.
Scientific acumen sufficient to lead a global MI function in the autoimmune space.
Excellent project management skills.
Strong cross-functional leadership and stakeholder management skills.
Proficiency with inquiry tracking systems, document management platforms, and data reporting tools (e.g., Power BI, Tableau, Excel).
Excellent written and verbal scientific communication skills, with experience presenting to executive leadership teams.
Excellent organizational, managerial, and communication skills.
Advanced degree (PhD, MD, PharmD, or equivalent) required.
Director level: 10 years of experience in MI or related MA roles within the pharmaceutical or biotechnology industry, with at least 3 years in a management or team leadership experience managing direct reports and/or matrixed teams.
Senior Director level: 12+ years of relevant experience in MI or related MA roles within the pharmaceutical or biotechnology industry, with at least 3 years of management or team leadership experience managing direct reports and/or matrixed teams.
Demonstrated ability to build, lead, and inspire high-performing teams.
Executive presence, excellent organization, communication, presentation, and stakeholder engagement skills.
Ability to operate effectively in a fast-paced, cross-functional environment.
Strong knowledge of applicable regulatory guidelines and standards.
Demonstrated leadership of MI functions through at least one product launch.
Direct experience managing outsourced MI operations and with MI inquiry management platforms.
Proficiency in scientific and clinical data review and interpretation.

Nice To Haves

Familiarity with ex-US regulatory frameworks and multi-country MI operations is preferred.
Experience in immunology, auto-immune disease, and/or rare disease highly desirable.

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.
Establish MI operational infrastructure, including inbound channels, escalation pathways, response turnaround standards, and documentation requirements prior to US launch.
Ensure global compliance with regulatory requirements and company policies and integration with the pharmacovigilance safety database, medical CRM, and document management system.
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 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.
Serves as the primary MI representative in cross-functional launch readiness governance. Provide regular MI performance reporting to MA leadership.
Partner with cross-functional teams including Pharmacovigilance, Regulatory Affairs, Commercial, and IT to support product launches and lifecycle management.
Monitor and analyze trends in medical inquiries to inform internal stakeholders (e.g., Medical Affairs, Commercial, Pharmacovigilance, Regulatory).
Develop and track key performance indicators (KPIs) to monitor performance, quality, and compliance of MI services.