Execute elements of clinical studies per quality standards (ICH/GCP, regulations, AbbVie policies).
Support Study Project Manager; lead cross-functional study team updates and CTMS upkeep.
Assist in developing study blueprint/protocol and documents (ICFs, eCRFs, IRT, CSR).
Assist vendor selection, scope, and oversight per AbbVie processes.
Generate study-related training for teams, sites, and vendors.
Identify and resolve escalated study issues; participate in process improvements.

🎯 Requirements

Bachelor’s Degree or OUS equivalent in nursing/science; RN licensure with ADN acceptable.
At least 4 years pharma/clinical research experience; strong core/technical competencies.
Strong communication skills; proficient with SOPs, ICH, regulations, ethics/compliance.
Clinical study initiation through completion preferred.
At least 3 years in clinical trial management.
English fluency (C1); remote position based in Madrid.

🎁 Benefits

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