Leads the planning and execution of phase 1-4 multicenter clinical studies, managing timelines, budgets, and resource planning. Oversees CROs and cross-functional teams to ensure high-quality trial delivery in compliance with global regulatory requirements.
Lundbeck
11 Remote Job Openings at Lundbeck
Develop and implement US regulatory strategies to ensure the successful development and approval of drug and biological products. Act as the primary FDA contact and manage the preparation and submission of regulatory documentation throughout the product lifecycle.
Lead the identification and implementation of MarTech investments and strategies to drive digital transformation and omnichannel customer engagement. Collaborate with cross-functional teams and external vendors to design technology frameworks that improve operational efficiency and customer experience.
Senior Medical Science Liaison Movement Disorders- South Central
Lundbeck
·
Full Time
·
13 days ago
Lundbeck
The Senior Medical Science Liaison (Sr MSL) provides advanced medical and scientific leadership in support of Lundbeck’s NeuroRare focus on multiple system atrophy. This role involves establishing partnerships with Key Opinion Leaders and generating actionable insights to inform evidence strategy and disease education.
Provide field-based medical leadership to support the NeuroRare focus on multiple system atrophy through strategic partnerships with external experts. Generate actionable scientific insights to inform evidence strategy, disease education, and launch readiness.
Senior Medical Science Liaison Movement Disorders - Northeast
Lundbeck
·
Full Time
·
13 days ago
Lundbeck
Provide field-based medical leadership to support the NeuroRare focus on multiple system atrophy through strategic partnerships with external experts. Generate actionable scientific insights to inform evidence strategy, disease education, and launch readiness.
Senior Medical Science Liaison Movement Disorders- West / South Central
Lundbeck
·
Full Time
·
a month ago
Lundbeck
Provide field-based medical and scientific leadership to support the NeuroRare focus on multiple system atrophy. Establish partnerships with Key Opinion Leaders to generate actionable insights that inform evidence strategy and launch readiness.
The Senior Director provides enterprise-wide leadership for Total Rewards and HR Operations in the US, shaping strategies that align with business objectives. They are responsible for the design, governance, and optimization of compensation, benefits, and HR technology while acting as a strategic advisor to executive leadership.
The Senior Director provides enterprise-wide leadership for Total Rewards and HR Operations, shaping strategies that align with business objectives and global priorities. They are responsible for the vision, governance, and optimization of compensation, benefits, and HR systems while acting as a strategic advisor to executive leadership.
The Director will develop and lead the U.S. patient advocacy strategy for rare disease therapeutic areas to support launch readiness and commercialization. They will build partnerships with patient advocacy groups and community leaders to drive disease awareness and address unmet patient needs.
The Director oversees the implementation of regulatory strategies for drug and biological products in the US, ensuring compliance and successful development. They lead a cross-functional team and serve as the primary regulatory contact for assigned products.
