AbbVie

Facilitate and participate in execution of study-related activities for a Phase I clinical study at
Maintain safety and confidentiality of study subjects; evaluate adverse events and manage safety
Review protocols and informed consent forms; identify and communicate potential issues.
Conduct nursing study activities per protocol in compliance with CFR, ICH, and GCP; coordinate with
Participate in quality and compliance initiatives; maintain source data in PIMS and resolve
Assist with protocol-specific training and onboard new nursing personnel; manage training materials

🎯 Requirements

Associate Degree in Nursing; Baccalaureate preferred.
5+ years of nursing experience and/or >4 years in a clinical research environment.

🎁 Benefits

AbbVie equal opportunity employer information and benefits disclosure included in posting.

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