Senior Director, Specialty Testing – Medical & Scientific Affairs
Beckman Coulter Diagnostics
Hartford (CT)
Presencial
USD 260.000 - 300.000
Jornada completa
14 días+
Generador de candidaturas
Una candidatura completa en un minuto — currículum y carta de presentación personalizados, listos para enviar.
Supera los filtros ATS
Ventajas ofrecidas por este puesto de trabajo
Medical/dental/vision insurance
401(k) plan
Paid time off
Descripción de la vacante
Beckman Coulter Diagnostics, a Danaher operating company, seeks a Senior Director of Medical & Scientific Affairs – Specialty Testing to set the vision and strategy for Specialty Testing, leading clinical research, product development, and regulatory activities. The role partners with external societies and leads HEPR efforts to shape outcomes and patient care on a global scale. This position may be remote with travel.
Formación
Excellent presentation, verbal, and written communication skills.
Strong leadership and collaboration across matrix organizations.
Minimum of 5 years of project management experience to set strategic goals and manage deliverables.
Experience in health economics, policy, and reimbursement (HEPR) considered a plus.
Responsabilidades
Steer and define global strategies for health economics, policy, and reimbursement for Beckman solutions.
Lead scientific and clinical positioning of products pre- and post-launch to ensure clinical utility.
Build and manage relationships with Key Opinion Leaders to drive scientific exchange.
Translate clinical insights into actionable guidance for product development teams.
Oversee pre-launch product initiatives, commercialization, and lifecycle management through education and evidence generation.
Conocimientos
Excellent communication
Leadership
Project management
Educación
Doctorate (M.D./Ph.D./Pharm.D./DNP)
Descripción del empleo
Beckman Coulter Diagnostics, a Danaher operating company, seeks a Senior Director of Medical & Scientific Affairs – Specialty Testing to set the vision and strategy for Specialty Testing, leading clinical research, product development, and regulatory activities. The role partners with external societies and leads HEPR efforts to shape outcomes and patient care on a global scale. This position may be remote with travel.
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