Similar Jobs
See allClinical Audit Associate
Kodiak Solutions
US
Risk Assessment
Regulatory Compliance
Electronic Medical Records
Regulatory Audit Coordinator
COG Research Foundation, LLC
US
Clinical Trials
FDA Regulations
ICH-GCP
Clinical Research Associate
Orca Bio
US
Oncology
Data Management
CTMS
Senior Clinical Trial Associate
Jobgether
US
Clinical Research
GCP
FDA Regulations
Associate Director, Regulatory Affairs
Zai Lab Limited
Global
Regulatory Affairs
Clinical Development
Regulatory Strategy
Role Overview:
- Lead clinical audits to assess compliance with regulations and AbbVie policies.
- Support GCP inspections and advance the global quality assurance system.
Responsibilities:
- Schedule, plan, and conduct clinical audits and communicate results within target timeframes.
- Review corrective action plans and track actions to completion.
- Promote continuous education on quality and clinical guidelines.
Qualifications:
- Bachelor's degree in science or healthcare with 3-5 years of biopharma experience.
- Strong knowledge of ICH-GCP, clinical trial regulations, and industry best practices.
- Effective project management and communication skills with willingness to travel internationally.
AbbVie
AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, neuroscience, and aesthetics. It is a large biopharmaceutical company committed to integrity, innovation, and community service.