Senior Medical Science Liaison, Movement Disorders

Lundbeck•Deerfield, IL

23d•Remote

About The Position

Do you want to join a team where the mission is meaningful, the challenges are complex, and you can directly see the results of your hard work? Lundbeck is a global biopharmaceutical company focusing exclusively on brain health. With more than 70 years of experience in neuroscience, we are committed to improving the lives of people with neurological and psychiatric diseases. Lundbeck employees are inspired and driven by our purpose to advance brain health and transform lives. Join us on our journey of growth! SUMMARY The Senior Medical Science Liaison (Sr MSL), Movement Disorders provides advanced, field-based medical and scientific leadership in support of Lundbeck’s NeuroRare focus on multiple system atrophy. This role serves as a strategic pre-launch scientific partner to external experts and internal stakeholders, generating high-quality, actionable insights that inform evidence strategy, disease education, portfolio decision-making, and launch readiness. The Sr MSL is expected to demonstrate outcome-oriented leadership, scientific depth, and insight generation that directly advances NeuroRare medical strategy, strengthens external scientific credibility, and shapes the disease environment.

Requirements

Accredited advanced degree in a health or life sciences–related field.
≥5 years of healthcare or related experience (industry, clinical practice, research, academic, or managed markets).
≥2 years of customer-facing Field Medical Affairs experience within a pharmaceutical, biotech, or life sciences organization.
Proven experience supporting pre-launch assets, including KOL identification, strategic mapping, trial site engagement.
Demonstrated ability to interpret complex scientific data and translate insights into meaningful scientific dialogue and decision-relevant insights.
Strong oral and written communication skills with the ability to influence without authority.
Proven ability to build trust, lead through scientific credibility, and operate effectively in a matrixed environment.
Track record of accountability, strategic thinking, and results orientation.
Proficiency in Microsoft Office applications (Word, Excel, PowerPoint, Outlook).
Driving is an essential duty of this job; must have a valid driver’s license with a safe driving record that meets company requirements.
The role is part of Lundbeck’s Vehicle Fleet Stipend Program and requires business use of a personal vehicle.

Nice To Haves

Doctoral degree (MD, DO, PharmD, PhD), an accredited advanced clinical degree (NP or PA), or a master’s degree in a health sciences–related field.
Experience and relationships in rare disease, Parkinson’s disease, neurodegenerative disorders, ataxia, autonomic disorders, or other related disease areas.
Background in clinical practice, academic research, or teaching.
Trusted and respected voice within the rare disease ecosystem, known for transparency, empathy, and meaningful community engagement.
Deep expertise in rare disease best practices.
Highly proactive and solutions-oriented, capable of driving organizational progress in ambiguous or unstructured settings.
Brings a mission-driven mindset — combining scientific rigor with empathy, credibility, and purpose to inspire cross-functional and external collaboration.
Maintains a broad and influential network within the rare disease ecosystem, effectively mobilizing partnerships and coalitions to accelerate shared goals.

Responsibilities

Establishes and sustains deep, longitudinal scientific partnerships with Key Opinion Leaders (KOLs), Centers of Excellence, and investigators working in multiple system atrophy.
Serves as a trusted scientific expert through high-quality, compliant scientific exchange that advances understanding of disease biology, unmet need, endpoints, and emerging evidence.
Acts as a primary generator of pre-launch actionable field medical insights by systematically testing scientific value narratives, differentiation hypotheses, and evidence gaps through external engagement.
Synthesizes and communicates high-quality insights with clear implications for evidence strategy, publication planning, disease education, and portfolio-level decision-making.
Ensures timely, accurate, and compliant documentation of insights in CRM systems in alignment with defined quality standards.
Partners closely with Medical Directors, Clinical Development, Evidence Strategy, and other cross-functional teams to align field execution with enterprise scientific priorities.
Connects external experts internally to support advisory boards, evidence generation activities, publications, and strategic initiatives.
Identifies and facilitates investigator-initiated trials (IITs), grant submissions, and research collaborations aligned with NeuroRare medical strategy.
Supports clinical development activities, including investigator identification and site outreach, as appropriate and compliant.
Delivers impactful, non-promotional disease education that advances recognition, diagnosis, and referral pathways across NeuroRare indications.
Ensures consistency, scientific rigor, and alignment of disease narratives and medical lexicon across field education activities.
Supports congress strategy execution by engaging in high-value scientific discussions, attending priority sessions, and facilitating strategic KOL interactions with Medical Leadership.
Maintains advanced knowledge of scientific and clinical developments in NeuroRare disease areas to inform education, insight generation, and evidence planning.
Demonstrates scientific and behavioral leadership through role modeling of best-in-class MSL execution, engagement quality, and compliance.
Actively contributes to Field Medical initiatives, workstreams, and process improvements that enhance scalability, quality, and impact.
Serves as a mentor and onboarding resource for new MSLs, as assigned, supporting development toward independent, high-quality field execution.
Completes all required training, administrative responsibilities, and documentation in accordance with Lundbeck policies and regulatory requirements on time.
Maintains full compliance with FDA, company, and governance standards with no critical findings.