Clinical Research Associate I
Core
Primary Sponsor point of contact for investigative sites, ensuring appropriate trial conduct, data integrity, compliance, and patient safety while driving study performance.
Role type
Junior Clinical Research Associate (Site Monitoring)
Builds
Clinical trial execution and data integrity for AbbVie's pipeline
Domain
Biopharmaceuticals / Clinical Research
Required skills
Site evaluation and monitoring, Protocol compliance, GCP/ICH Guidelines knowledge, Patient recruitment and retention, Risk assessment, Data quality assurance, Regulatory inspection readiness, Investigator management
Preferred skills
Health-related degree (Medical, Nursing, Pharmacy), Therapeutic area knowledge, Clinical research coordinating experience, Data management experience
Technologies
Site engagement tracking tools, Clinical trial management systems
Responsibilities
Conduct routine on-site and off-site monitoring, Align and train site staff and principal investigators, Ensure audit and regulatory inspection readiness, Manage investigator payments, Identify and evaluate potential investigators/sites, Resolve site risk signals and implement corrective actions, Ensure timely submission of safety events and data
Seniority
Entry-level, hands-on IC