Associate Director, Medical Affairs Content Development

Join Us in Tackling Autoimmune Disease at Its Root

At Vor, we believe science can do more than manage symptoms. It can change the course of disease. 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.

When you join Vor, you’re not just working on a medicine. You’re part of a mission to redefine the future of autoimmune care.

Why Work at Vor?

Impact: Contribute directly to a medicine with best-in-disease Phase 3 results in myasthenia gravis and expansion into multiple autoimmune diseases.

Growth: Be part of a rapidly scaling company with opportunities to grow your career in science, clinical development, commercial strategy, and beyond.

Innovation: Work on a platform with potential beyond one indication — a therapy that has already shown consistent results across lupus, IgA nephropathy, and Sjögren’s syndrome.

Belonging: Join a culture where every voice is heard, and where our shared mission unites us across functions and geographies.

Who we are looking for:

The Associate Director, Content Development will lead the design, creation, and execution of high-quality scientific and medical content to support Medical Affairs strategy across multiple therapeutic areas. This individual will be responsible for ensuring accuracy, consistency, and scientific integrity across core communication platforms, training resources, publications support, and external-facing educational materials.

The role requires strong scientific writing and communication skills, the ability to translate complex data into clear messaging, and close collaboration with internal stakeholders and external partners.

Key Responsibilities

Content Strategy & Development

• Lead the creation and maintenance of the Scientific Communication Platform and core content decks.
• Develop medical and scientific content across a range of formats: slide decks, FAQs, training modules, disease education resources, and digital tools.
• Partner with Medical Directors, MSLs, and cross-functional colleagues to ensure alignment with scientific strategy and data integrity.
• Adapt global content for regional or local use, ensuring consistency in scientific messaging.

Publications & Data Dissemination Support

• Contribute to the publications planning process, ensuring integration of data into medical content platforms.
• Support congress activities, including development of scientific booth materials, symposia slides, and post-congress summaries.
• Collaborate with external authors, agencies, and vendors to deliver high-quality, compliant materials.

Medical Education & Training

• Create internal training materials for Medical Affairs and field medical teams, ensuring consistent understanding of scientific data and disease state.
• Support external education initiatives, including advisory board content, speaker programs, and medical symposia.
• Ensure all content is scientifically rigorous, compliant, and tailored to the needs of the audience.

Cross-Functional Collaboration

• Partner with Clinical Development, Regulatory, Commercial, and Patient Advocacy to ensure consistency in data interpretation and messaging.
• Collaborate with Field Medical teams to identify content gaps and develop resources that enhance field impact.
• Serve as a content development lead within scientific review committees (MLR/MRC) to ensure efficient review and approval.

Skills & Competencies

• Exceptional ability to synthesize and communicate complex scientific and clinical information clearly and persuasively.
• Strong project management skills with the ability to manage multiple priorities and timelines.
• Highly collaborative, with proven ability to work across diverse teams and functions.
• Knowledge of scientific exchange, compliance standards, and medical affairs best practices.
• Adept at working with agencies, vendors, and authors to produce publication-quality deliverables.
• Attention to detail with a high bar for scientific rigor and accuracy.

Education & Experience

• Advanced degree in a scientific or medical discipline (PharmD, PhD, MD, or equivalent) required.
• 6–8 years of experience in medical affairs, medical communications, or scientific writing within biotech/pharma.
• Demonstrated success in developing medical content, training resources, and communication platforms.
• Experience supporting late-stage development and product launches preferred.
• Familiarity with digital tools, scientific publication standards (GPP, ICMJE), and compliance frameworks.

At Vor, we support our team with robust benefits, including comprehensive health coverage, flexible paid time off, generous parental leave, and a competitive 401(k). From education assistance to wellness resources and financial security, we invest in your well-being so you can thrive at work and beyond.

As an equal opportunity employer, we at Vor Bio know that diversity inspires innovation, inclusiveness, and creativity. We invite you to come as you are. All applicants will be considered for employment agnostic to race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

Please visit our website at https://www.vorbio.com/ for more information.