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.
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.
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.
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.
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.
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.
The Vice President will own the global brand strategy and marketing organization, leading the company through the launch of vidofludimus calcium. They will build the marketing function from the ground up, managing budgets, agency partners, and cross-functional collaboration with medical and regulatory teams.
