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Dyne Therapeutics · 2 hours ago

Director, Medical Information

United States

Full-time

Remote

Director/Executive

$183K/yr - $255K/yr

10+ years exp

Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. The Director, Medical Information is responsible for establishing and leading the medical information function to ensure timely, accurate, and compliant scientific responses to inquiries from healthcare professionals.

BiotechnologyHealth CareMedicalPharmaceutical

Growth Opportunities

Responsibilities

Establish and lead the medical information function, including strategy, processes, and execution

Establish scalable medical information infrastructure, including inquiry intake, documentation, and response workflows

Oversee the implementation and training of the medical inquiry intake portal and call center vendors and manage relationships going forward

Develop high-quality medical information response documents (standard response letters, FAQs, backgrounders) and maintain medical information content aligned with product labeling, clinical data, and evolving scientific evidence

Ensure responses are scientifically accurate, balanced, up-to-date, and compliant with regulations

Ensure appropriate escalation and coordination of safety, quality, and off-label inquiries

Analyze inquiry trends to identify knowledge gaps, unmet medical needs, and opportunities to inform medical strategy

Monitor metrics and quality indicators to ensure continuous improvement and compliance

Qualification

Doctorate degreeMedical information experienceRegulatory compliance knowledgeScientific writing skillsOrganizational capabilitiesProcess-building skillsJudgment in inquiriesWork in biotechAttention to detailVerbal communication skills

Required

Doctorate degree (MD, PhD, PharmD) with 10+ years of experience in medical information or medical affairs in rare diseases, neuromuscular diseases, or a related field

Strong understanding of regulatory, compliance, and pharmacovigilance requirements

Excellent scientific writing and verbal communication skills

Strong organizational and process-building capabilities

High attention to detail and commitment to compliance and scientific integrity

Ability to work effectively in a matrixed, fast-paced biotech environment

Strong judgment in handling complex or sensitive inquiries