Associate, Study Management II

• Execute one or more elements of clinical studies in compliance with ICH/GCP, global regulations, and AbbVie policies and procedures
• Support the Study Project Manager in leading the cross-functional study team
• Prepare Clinical Study Team meeting agendas and minutes
• Provide regular study-status updates to the cross-functional team and stakeholders and keep the CTMS up to date
• Support development of clinical study blueprints/protocols and associated systems and documents, including informed consent forms, eCRFs, IRT, and CSR
• Support vendor selection, scope development, management, and oversight in compliance with AbbVie processes and applicable regulations
• Generate study-related training for study teams, study sites, and vendors
• Proactively identify, resolve, and/or escalate study-related issues
• Participate in process improvement initiatives

• Bachelor’s Degree or OUS equivalent degree required, typically in nursing or scientific field
• Registered Nurse licensure with Associate’s Degree in Nursing with relevant experience is also acceptable
• Two years of Pharma-related/clinical research related experience or professional equivalent desired
• Analytical and critical thinking skills
• Good communication skills

• Equal opportunity employer
• Committed to operating with integrity, driving innovation, transforming lives and serving the community