
Medical Affairs Director – Movement Disorders
Posted 20 hours ago

Posted 20 hours ago
This is a fully remote position, open to applicants in Massachusetts.
• Provide strategic medical leadership for Multiple System Atrophy (MSA).
• Support launch readiness and execution across the U.S. Medical Affairs organization.
• Shape and advance U.S. medical strategy utilizing scientific evidence and insights from external stakeholders.
• Collaborate with Commercial, Patient Advocacy, Market Access, Regulatory, Clinical Development, Pharmacovigilance, and other stakeholders to co-create launch strategies.
• Assist in launch readiness, lifecycle planning, and integrated evidence generation strategies.
• Convert clinical data and scientific insights into stakeholder engagement and brand-planning strategies.
• Establish and maintain relationships with investigators, KOLs, advocacy leaders, and healthcare professionals.
• Represent U.S. Medical Affairs in scientific forums and stakeholder engagements.
• Keep track of disease-area trends, competitor activities, and policy developments.
• Develop and implement an integrated U.S. medical communications strategy.
• Co-create the scientific narrative, clinical value story, lexicon, data story, key messages, evidence summaries, and communication themes in collaboration with Global Medical Affairs.
• Oversee U.S.-specific publication strategies and priorities.
• Organize and implement U.S. congress activities, including data rollouts, abstracts, posters, oral presentations, symposia, booths, and communications.
• Create stakeholder mapping and engagement plans.
• Manage U.S. medical materials, slide decks, FAQs, scientific response documents, congress assets, field medical materials, training content, data visualizations, and digital scientific content.
• Support Field Medical scientific readiness and training.
• Act as a medical reviewer in the promotional review process.
• Oversee medical writing agencies, publication vendors, freelancers, congress vendors, budgets, timelines, and deliverables.
• Drive cross-functional alignment, scientific excellence, external engagement, and execution of the U.S. medical strategy.
• Accredited advanced scientific or clinical degree (MD, PharmD, PhD or MS).
• 5+ years of progressive, non-field-based Medical Affairs experience within the pharmaceutical or biotech industry, or at an agency supporting these sectors.
• A minimum of 2+ years contributing to medical strategy development, launch readiness, scientific communications, publication planning, and congress management.
• Experience in designing and executing Medical Education programs (CME and non-CME).
• Strong understanding of clinical trial data, evidence generation, publication practices, and therapeutic-area strategies.
• Experience in developing publication plans, congress materials, scientific platforms, and medical content.
• Knowledge of compliance requirements, publication ethics, and medical/legal/regulatory review processes.
• Experience serving as a medical reviewer for promotional materials.
• Strong analytical thinking, problem-solving, and data-driven decision-making capabilities.
• Proven experience in building collaborative cross-functional relationships and influencing without formal authority.
• Ability to manage multiple priorities in a fast-paced environment.
• Exceptional communication skills for articulating complex scientific information clearly and persuasively.
• Demonstrated integrity, professionalism, and a commitment to ethical standards.
• Authentic, long-term engagement within the rare disease community.
• Capability to collaborate with patient advocacy groups, patients, caregivers, clinicians, and industry stakeholders.
• Deep understanding of rare disease best practices, access and policy considerations, media engagement, and patient support ecosystems.
• Strong external network among rare disease leaders, clinical societies, and alliances.
• Highly proactive and adaptable leadership in evolving, data-limited environments.
• Willingness and ability to travel up to 35% domestically; occasional international travel may be required.
• Eligibility for a 25% bonus target based on company and individual performance.
• Opportunity to participate in the company’s long-term incentive plan.
• Flexible paid time off (PTO).
• Comprehensive medical, dental, and vision health benefits.
• Company match for 401k contributions.
• Reasonable accommodations during the employment application process.
• Commitment to equal employment opportunity in the workplace.
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