Director, Scientific Communications

🔥 18 minutes ago

🇺🇸 United States – Remote

💵 $230k - $255k / year

⏰ Full Time

🔴 Lead

🗣️ Communications

👻 Ghost score 0%

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Immunic Therapeutics

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2016

🏥 Healthcare

💼 Consulting

⚖️ Legal

Healthcare • Consulting • Legal

Immunic Therapeutics is a late-stage biotechnology company focused on developing novel, orally administered small-molecule therapies for chronic inflammatory and autoimmune diseases, with particular programs targeting multiple sclerosis and celiac disease. The company advances differentiated clinical-stage programs (e. g. , vidofludimus calcium, IMU-856, IMU-381) aiming to provide efficacious, safe, and well-tolerated oral treatment options for neurologic and gastrointestinal immune-mediated conditions, while pursuing regulatory protections and commercialization pathways.

📋 Description

• Lead and oversee integrated scientific communications plans for vidofludimus calcium and Immunic’s broader pipeline • Translate Medical Affairs priorities and evolving evidence into workplans, deliverables, timelines, and execution roadmaps • Operationalize and maintain the scientific platform, lexicon, dissemination framework, and core narrative • Manage publication planning, steering committee activities, author engagement, abstracts, posters, and manuscripts • Ensure publications and communications follow Good Publication Practice, ICMJE criteria, industry standards, and internal review processes • Lead congress and field medical content planning, including messaging, debriefs, modular resources, training content, FAQs, and evidence summaries • Partner with Field Medical leadership to incorporate insights and maintain timely, relevant resources • Manage literature surveillance and synthesize competitive intelligence and external scientific developments • Recommend content updates, communication priorities, and risk-mitigation actions • Establish scalable content standards, templates, review processes, version control, and lifecycle practices • Collaborate with Medical Affairs, Medical Review, Medical Information, HEOR, Clinical Development, Market Access, Commercial, Legal, Compliance, Regulatory, external experts, and agencies • Select, onboard, manage, and hold external agencies and vendors accountable for quality, timelines, budgets, and deliverables • Provide operational leadership to external partners and cross-functional teams

🎯 Requirements

• Advanced scientific or clinical degree required, such as PhD, PharmD, MD, or equivalent • Strong scientific writing and communication background • 8+ years of relevant experience in scientific communications, publications, Medical Affairs, medical communications, or related biopharma functions • Experience developing and executing publication plans, scientific platforms, congress plans, manuscripts, abstracts, posters, presentations, and other evidence dissemination deliverables • Strong working knowledge of Good Publication Practice, ICMJE authorship criteria, publication ethics, medical/legal/regulatory review processes, and industry expectations for transparency and scientific integrity • Experience selecting, managing, and leading external agencies, medical writers, publication partners, and other vendors • Ability to lead through influence, implement strategic direction, oversee complex cross-functional workstreams, and build scalable capabilities • Excellent written and verbal communication skills, with ability to translate complex science into clear, accurate, audience-appropriate content • Strong prioritization, project management, and problem-solving skills • US work authorization required

🏖️ Benefits

• Equity • Bonus • Equal Opportunity Employer committed to a diverse, inclusive, and equitable workplace

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