Medical Affairs Scientific Communications Director – Movement Disorders

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Cookie Information

51 - 200 employees

Founded 2011

🤝 B2B

📋 Compliance

B2B • Compliance • Marketing

Cookie Information is a leading consent management platform that simplifies the process of collecting user consent for cookies and tracking on websites and mobile applications. It is designed for marketers to ensure compliance with privacy regulations like GDPR, while enhancing marketing performance. The platform provides customizable cookie banners that integrate with various systems, enabling businesses to manage cookie consent effectively and maintain regulatory compliance without sacrificing their marketing capabilities.

📋 Description

• Lead the strategic development and execution of scientific communication plans for MSA that support launch readiness • Lead and oversee publication planning, congress strategy, data dissemination, medical and digital content development, scientific platform development, promotional medical review, agency/vendor management, budget oversight, and compliance review • Partner closely with HEOR, Commercial, Customer insights & analytics, Patient advocacy, Clinical Development, Compliance, Legal, Medical Affairs Operations, and Medical Affairs teams and external experts • Drive cross-functional alignment, ensure scientific excellence, and elevate Lundbeck’s presence and credibility within the Multiple System Atrophy community • Develop and execute an integrated US medical communications strategy aligned to overarching brand and development objectives, with measurable impact • Develop and maintain the scientific narrative, clinical value story, lexicon, data story, key messages, evidence summaries, and communication themes • Ensure consistent, accurate, and balanced communication of clinical data across materials • Own US publication strategy and priorities; ensure alignment and integration with global publication plans • Oversee development of all US medical materials, medical slide decks, FAQs, scientific response documents, congress assets, field medical materials, training content, data visualizations, digital scientific content, and other non-promotional medical resources ensuring scientific accuracy, regulatory compliance, and strategic alignment

🎯 Requirements

• Accredited advanced scientific or clinical degree (MD, PharmD, or PhD) • 5+ years of progressive, non-field-based Medical Affairs experience within pharmaceutical or biotech industry or at an agency that supports the pharmaceutical or biotech industry • Minimum 2+ years contributing to medical strategy development, launch readiness, scientific communications, publication planning, and congress management • Demonstrated experience designing and executing Medical Education programs (CME and non-CME) • Strong understanding of clinical trial data, evidence generation, publication practices, and therapeutic-area strategy and translate insights into strategic recommendations • Experience 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, ensuring compliance and scientific rigor • Strong analytical thinking, problem-solving capability, and data-driven decision-making skills • Demonstrated success building collaborative cross-functional relationships and influencing without authority • Experience managing multiple priorities in a dynamic environment • Exceptional communication skills with ability to convey complex scientific information clearly and persuasively • Demonstrated integrity, professionalism, and commitment to ethical standards • Authentic, long-term engagement within the rare disease community, viewed as a trusted and mission-driven partner • Demonstrated ability to collaborate respectfully and effectively with patient advocacy groups (PAGs), 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 across rare disease leaders, clinical societies, and alliances (e.g., Rare Disease Caucus, PFDD Consortium, FDA Rare Disease Center of Excellence) • Highly proactive and adaptable leader capable of operating effectively in evolving, data-limited environments.

🏖️ Benefits

• flexible paid time off (PTO) • health benefits to include Medical, Dental and Vision • company match 401k

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