United States$220K - $300K per year10+ yrs expOthers
Lead translational medicine and pharmacology strategy across the pipeline, with an initial focus on the Phase 3 vidofludimus calcium program for multiple sclerosis, including biomarker strategy, mechanism-of-action work, and PK/PD and exposure-response analyses. Partner across clinical, regulatory, discovery, and medical affairs teams to support development decisions, regulatory interactions, scientific communications, business development, and growth of the translational medicine function.
United States$180K - $230K per year10+ yrs expProduct
Lead project management for drug development program teams and strategic initiatives, coordinating integrated plans, cross-functional execution, governance, and readiness for Phase 3, regulatory submissions, and commercial launch. Monitor risks, resources, dependencies, and decisions; provide leadership updates and drive mitigation and continuous improvement.
United States$310K - $350K per year10+ yrs expMarketing
The Vice President will lead an integrated strategy for patient advocacy, corporate communications, and government affairs to shape the company's reputation and strategy. They will serve as a senior advisor to the executive team and build a high-performing team to manage external engagement and clinical milestone communications.
United States$200K - $270K per year10+ yrs expMarketing
The Senior Director will develop and execute an integrated corporate communications strategy to strengthen Immunic's reputation and elevate awareness of its science. They will serve as a trusted advisor to senior leadership while managing media relations, internal communications, and crisis-management capabilities.
United States$170K - $210K per year5-10 yrs expHealthcare
The Associate Director will build and lead Medical Information and Medical Review capabilities, serving as a subject-matter expert for scientific content and communications. They will manage inquiry responses, ensure the integrity of promotional and non-promotional materials, and partner with cross-functional teams to support regulatory and launch readiness.
United States$230K - $270K per year10+ yrs expHealthcare
The Director will establish and lead the HEOR capability within Medical Affairs, developing integrated value-evidence strategies to support clinical development and launch readiness. They will partner cross-functionally to generate real-world evidence and economic models that address the needs of payers, HTA bodies, and healthcare systems.
United States$230K - $255K per year10+ yrs expOthers
The Director will lead the implementation of integrated scientific communications plans, including publications, congress activities, and field medical content. They will operationalize the scientific narrative and manage cross-functional collaborations to ensure compliant and rigorous communication deliverables.
United States$180K - $210K per year5-10 yrs expHealthcare
Provide operational leadership for the planning, execution, and close-out of global clinical studies while managing cross-functional teams and CROs. Ensure study delivery remains within budget, on schedule, and in full compliance with regulatory standards and protocols.
United States$330K - $410K per year10+ yrs expOthers
The Vice President of Pharmacovigilance is responsible for establishing and overseeing global drug safety strategies, policies, and operations. This role involves leading cross-functional governance, managing regulatory filings, and ensuring compliance with international safety standards.
United States$285K - $340K per year10+ yrs expOthers
The Vice President of Market Access will lead the U.S. market access strategy, including pricing, contracting, and distribution for the launch of vidofludimus calcium. They will also build and manage a high-performing team to drive payer strategy and ensure successful commercialization.
