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(R-037) Executive Medical Director

Detalles del Trabajo

Barcelona, Catalonia, España
Alexion Pharmaceuticals,Inc.
03.08.2025
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Some opportunities happen only once in a lifetime - like a job where you have the chance to change lives. At Alexion, people living with rare and devastating diseases are our Guiding Star. We are driven to continuously innovate and create meaningful value in all we do to help patients and families fully live their best lives. We value the uniqueness and diversity of our employees and recognize that nurturing the diverse perspectives and strengths of our people translates into innovative breakthroughs for patients.Executive Medical Director
Location:
Hybrid, BarcelonaReports To:
Vice President, Clinical Development, NF1 & Bone Metabolism, AlexionWhat you will do
The Executive Medical Director is responsible for overseeing multiple global programs, providing guidance to Medical Directors and Clinical Development Scientists, and participating in strategic teams. May manage senior medical staff and support other medical personnel reporting indirectly. Supports the VP TA Head and acts as their delegate in scientific and governance meetings.Responsibilities
Lead and oversee multiple program teams, driving the execution of clinical studies and research strategies.Represent Clinical Development on global teams and in management presentations, advancing understanding of therapies for rare diseases.Develop and mentor Medical Directors, CDS, and fellows;
oversee clinical development strategies and documentation including protocols and regulatory submissions.Provide scientific and medical input to R&D, commercial, and business development;
support due diligence activities.Represent Alexion Clinical Development to internal and external stakeholders.Oversee clinical components of the Clinical Development Plan, serve as medical expert for study teams, and contribute to regulatory documents.Coordinate with other R&D functions to align program strategies and clinical study design.Stay informed on scientific, clinical, and regulatory developments impacting development plans.Contribute to white papers, expert reports, and regulatory responses.Support business development through due diligence and research collaborations.Evaluate disease landscapes and competitive environments to inform strategy.Work with advisory boards and cross-functional teams;
may supervise other medical monitors.Requirements
10+ years in clinical development, with expertise in research, regulatory, and product development.Peer-reviewed publications.Excellent communication skills.Attention to detail.
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