Remote Senior Clinical Trial Lead — Madrid

ABBVIE

Madrid

Híbrido

EUR 48.000 - 72.000

Jornada completa

14 días+
Generador de candidaturas

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Descripción de la vacante

AbbVie seeks a qualified professional to execute and support clinical studies from Madrid in a remote capacity. The role requires SOP/ICH knowledge, regulatory compliance, and collaboration with cross-functional teams to ensure quality study conduct.

Candidates should have 4+ years in pharma-related research and at least 3 years in trial management, with RN or science background. This position is based in Madrid and offers remote work within Spain.

Formación

  • Bachelor’s degree or equivalent in nursing or scientific field.
  • RN licensure with ADN with relevant experience acceptable.
  • At least four years in pharma-related/clinical research.
  • Experience with SOPs, ICH, global regulations, ethics and compliance.
  • Preferred exposure from initiation to study completion.
  • ≥3 years in clinical trial management.

Responsabilidades

  • Execute elements of clinical studies in compliance with quality standards (ICH/GCP, global regulations, AbbVie policies).
  • Support Study Project Manager in leading cross-functional study team; prepare agendas/minutes; update study status and CTMS.
  • Assist development of study blueprint/protocol and documents (informed consent forms, eCRFs, IRT, CSR).
  • Assist vendor selection, scope development, management and oversight of external vendors per AbbVie processes.
  • Generate study-related training for study team, sites and vendors.
  • Identify and resolve or escalate study-related issues proactively.
  • Participate in process improvement initiatives.

Conocimientos

Pharma/clinical research
Clinical study management
Regulatory compliance
GCP/ICH knowledge

Educación

Bachelor’s degree
Nursing license

Herramientas

CTMS experience
eCRF systems

Descripción del empleo

AbbVie seeks a qualified professional to execute and support clinical studies from Madrid in a remote capacity. The role requires SOP/ICH knowledge, regulatory compliance, and collaboration with cross-functional teams to ensure quality study conduct.

Candidates should have 4+ years in pharma-related research and at least 3 years in trial management, with RN or science background. This position is based in Madrid and offers remote work within Spain.

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