Define and drive operational strategies and deliverables for one or more clinical studies
Execute clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, AbbVie
Manage budget, timelines, study issues; bring scientific acumen, technical expertise and global
Lead cross-functional Clinical Study Team
Manage vendors and external stakeholders including site staff, Key Opinion Leaders, patient groups
Coach and support cross-functional team members; delegate and empower appropriately

🎯 Requirements

Bachelor's Degree or equivalent degree required
6 years of demonstrated pharma-related and/or clinical research related experience or equivalent
Preferred exposure in study initiation through study completion in Phase 1-4 or medical device

🎁 Benefits

Comprehensive benefits package including paid time off (vacation, holidays, sick) /n

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