Medical Affairs Scientific Communications Director – Movement Disorders

🕒 vor 3 Monaten

🌽 Illinois – Remote

🌽 Illinois – Remote

💵 $260.000 - $290.000 / Jahr

⏰ Vollzeit

🔴 Experte

🗣️ Kommunikation

👻 Geisterscore 35%

Was es bedeutet: wie wahrscheinlich diese Stelle offen bleibt, ohne dass aktiv eingestellt wird.So liest du es: 60 % oder höher heißt, wir halten das für einen Geisterjob. Niedrigere Werte sind weniger bedenklich.Wie wir werten: Dauer offen, Neuveröffentlichungen, offene Stellen vs Teamgröße, wie schnell Stellen geschlossen werden, und ob ein Gehalt angegeben ist.Hinweis: eine Schätzung aus öffentlichen Daten, kein Urteil über das Unternehmen. Echte Stellen können hoch punkten, nutze es also als Hinweis, nicht als Fakt.

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Lebenslauf hochladen

Lundbeck

WebsiteLinkedInAlle Stellen

5001 - 10000 Mitarbeiter

Gegründet 1915

🏥 Gesundheitswesen

🏭 Fertigung

💼 Beratung

💰 €566.373.927 Post-IPO Debt - Lundbeck im 2025-05

Healthcare • Manufacturing • Consulting

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Beschreibung

• 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

🎯 Anforderungen

• 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.

🏖️ Vorteile

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