Clinical Trial Associate I

Abbott seeks a Clinical Trial Associate I to provide administrative and project management support for clinical trial execution. The role involves coordinating with clinical sites, managing study documentation, tracking supplies, and supporting the Clinical Affairs team to ensure successful study implementation.

Responsibilities

• Review documents for completeness and compliance with protocols, SOPs, and regulations
• Coordinate with clinical study sites on start-up, execution, and close-out activities
• Create and maintain study trackers for enrollment, supplies, samples, and site information
• Order, track, and manage clinical supplies and investigational product materials
• Support case report form development and electronic data system testing

Requirements

• Bachelor's degree in life sciences or related field; or Associate's degree with 2+ years relevant experience
• Knowledge of clinical research principles, GCP, and ICH guidelines
• Proficiency with Microsoft Office (Word, Excel, Outlook) and internet search tools
• Authorization to work in United States without sponsorship
• Strong written and verbal communication skills
• Excellent organizational and attention to detail
• 1+ year clinical research experience preferred

Compensation: $50,700–$101,300 base