Clinical Trial Associate I
Abbott · Madison
Clinical OperationsFull-time$51k–$101kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
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.
What they're looking for
- 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
What you'll be doing
- 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
Privacy & handoff
This role links to Abbott's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.