Senior Clinical Trial Manager — Remote (Madrid)

AbbVie

Madrid

Presencial

EUR 70.000 - 90.000

Jornada completa

14 días+
Generador de candidaturas

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Descripción de la vacante

AbbVie seeks a full-time, remote-position professional based in Madrid to execute clinical studies in line with ICH/GCP and regulatory standards. You will support the Study Project Manager, lead cross-functional study teams, and oversee CTMS and vendor relationships from Madrid.

You will help develop study blueprints, create training for sites and vendors, and proactively identify and resolve issues while driving process improvements within AbbVie's clinical operations.

Formación

  • Bachelor's degree in nursing or science; RN licensure acceptable.
  • Minimum four years in pharma/clinical research with core competencies.
  • Fluent in English; strong communication and cross-functional collaboration.
  • Experience in clinical trial management; knowledge of SOP/ICH/regulatory requirements.

Responsabilidades

  • Execute one or more elements of clinical studies in compliance with quality standards (ICH/GCP, global regulations and AbbVie policies).
  • Support Study Project Manager in leading cross-functional study team (Agenda/Minutes, status updates).
  • Assist in vendor selection and oversight; ensure CTMS is up to date.
  • Generate study-related training for study team, sites and vendors; support training materials.
  • Identify and resolve study-related issues; participate in process improvements.

Conocimientos

Communication skills
Clinical study management
ICH knowledge
Vendor management
Study protocol execution
English fluency

Educación

Bachelor’s degree in nursing or science
RN licensure or equivalent

Herramientas

CTMS

Descripción del empleo

AbbVie seeks a full-time, remote-position professional based in Madrid to execute clinical studies in line with ICH/GCP and regulatory standards. You will support the Study Project Manager, lead cross-functional study teams, and oversee CTMS and vendor relationships from Madrid.

You will help develop study blueprints, create training for sites and vendors, and proactively identify and resolve issues while driving process improvements within AbbVie's clinical operations.

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