The Medical Science Liaison will manage key opinion leaders in the eye care field, providing scientific education and gathering actionable insights to shape medical strategy. They are responsible for conducting compliant scientific exchanges, supporting clinical trials, and representing the company at medical meetings.
The District Leader is responsible for leading, coaching, and developing a team of sales professionals to drive performance and achieve sales goals within their assigned territory. They will champion a culture of excellence, manage customer relationships, and ensure compliant execution of sales strategies.
The Territory Leader is responsible for driving the launch and growth of XDEMVY through expert account management and clinical education within the eye care sector. They must execute sales strategies, monitor performance metrics, and foster strong relationships with key stakeholders to maximize territory results.
The Regional Director will lead and mentor a team of Medical Science Liaisons to drive medical strategy and scientific engagement within the East region. They will oversee cross-functional collaboration, ensure regulatory compliance, and manage relationships with Key Opinion Leaders and Eye Care Practitioners.
The Medical Science Liaison will manage key opinion leader relationships in the eye care field and provide scientific education on disease states. They are responsible for collecting actionable insights to shape medical strategy and supporting clinical trial initiatives within their assigned territory.
The Director will create early development clinical plans, study designs, and essential regulatory documents while leading cross-functional study teams. They are responsible for overseeing study investigators, interpreting clinical data, and engaging with KOLs and regulators to drive program strategies.
Lead the toxicology and translational science strategy to bridge discovery and clinical development from concept through early clinical studies. Oversee GLP and non-GLP studies at CROs and author toxicology sections for regulatory submissions such as INDs and NDAs.
Provides strategic and scientific leadership for all clinical programs from first-in-human through registration and approval. Oversees Clinical Sciences, Operations, and Biostatistics while partnering cross-functionally to drive efficient and rigorous clinical work.
Lead the end-to-end drug product manufacturing strategy and oversee external CDMO operations from late-stage development through commercialization. Ensure reliable supply and scalability while managing critical manufacturing issues and cross-functional alignment on CMC strategy.
Lead the development of clinical strategies and ensure the efficient execution of clinical development plans for assigned programs. Act as the primary author for clinical trial protocols and manage communications with CROs, sites, and health authorities.
