Clinical Research Associate
Sacramento, CAFull-time
Behavioral Health Market Context
Qualifications
- •Identifies, evaluates and recommends new/potential investigators/sites on an on going basis
Responsibilities
- •Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol
- •Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes
- •Ensures regulatory inspection readiness at assigned clinical sites
- •Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations
- •1 more items(s)