AbbVie seeks a Study Management Associate III to lead clinical trial execution across Phase 0-4 studies in a global, cross-functional environment. The role involves independent management of study activities from inception through closure, vendor oversight, recruitment strategy, and compliance with regulatory standards.
Responsibilities
Lead cross-functional study teams and manage strategic activities from trial inception through closure
Oversee vendor management including RFP development, selection, and performance monitoring
Develop and execute global recruitment strategies with risk mitigation planning
Co-develop and manage study documentation including protocols, regulatory submissions, and compliance materials




Provide stakeholder training and support process improvement initiatives
Requirements
Bachelor's degree or equivalent international qualification
Minimum 4 years progressive pharmaceutical or clinical research experience
Proficiency with EDC, IRT, CTMS, and eTMF systems
Strong knowledge of ICH/GCP guidelines and regulatory compliance procedures
Excellent analytical, organizational, and time management skills
Fluent English proficiency (oral and written) for general communications
Experience with study initiation through completion activities preferred

📌 Study Management Associate Iii (Xico)
🏢 Abbvie
📍 Xico