Más empleos:
Director, Nonclinical and Clinical Pharmacology Writing
Trabajo disponible en:
08001, Barcelona, Cataluna, España
Publicado en 2025-12-11
Empresa:
JR Spain
Tiempo completo
posición Publicado en 2025-12-11
Especializaciones laborales:
-
Servicios Médicos
Ciencia Médica, Investigación clínica, Medical Science Liaison
Descripción del trabajo
Director, Nonclinical and Clinical Pharmacology Writing, Barcelona
Client: Alexion Pharmaceuticals, Inc.
Location:
Barcelona, Spain
Job Category: Other
EU Work Permit
Required:
Yes
Job Reference: 163299174470018662432460
Job Views: 1
Posted: 23.07.2025
Expiry Date: 06.09.2025
Job Description:
Location:
Barcelona, Spain
Job Reference: R-211288
Date Posted: 06/23/2025
Position Overview:
This position is responsible for the timely delivery of high-quality nonclinical and clinical pharmacology (NCCP) regulatory documents supporting the clinical development portfolio role involves leading NCCP writing activities across disease areas or clinical development programs with limited supervision.
Key Responsibilities:
Develop and implement document strategies for NCCP regulatory documents, including protocols, Investigator’s Brochures, and module 2 summaries for IND/CTA/NDA submissions.
Contribute to briefing packages, responses to health authority inquiries, and other submission documents.
Author and manage high-quality NCCP medical writing, ensuring scientific accuracy, clarity, and regulatory compliance.
Review documents prepared by others to ensure quality and adherence to standards.
Mentor medical writing team members to ensure quality and efficiency.
Maintain adherence to SOPs and regulatory requirements in collaboration with cross-functional teams.
Qualifications:
Minimum 10 years of regulatory medical writing experience with global submissions.
Ability to summarize complex data and produce regulatory documents.
Excellent communication, presentation, and Microsoft Office skills.
Thorough knowledge of global regulatory requirements and ICH/GCP guidelines.
Experience managing internal and external medical writers and training staff.
Strong ethical standards and professionalism.
Preferred Qualifications:
PhD or MS in life sciences or relevant field.
Experience with global clinical studies, regulatory submissions, and rare diseases.
Skills in project management, planning, and negotiation.
Ability to adapt and innovate in changing environments.
Additional Information:
This role is primarily office-based. Candidates must be able to use a computer, communicate via phone and electronic messaging, and collaborate effectively during standard business hours.
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