Senior Clinical Research Nurse
AbbVieRemotely
gcpclinical researchnursingichpimscfrinformed consent
Job Description
📋 Description
- 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.