Clinical Research Associate I
Abbott · Abbott Park, IL +1 more
Clinical OperationsFull-time$61k–$123kCompany career page
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Role summary
Abbott seeks a Clinical Research Associate I to support clinical trial sites through study lifecycle management, ensuring protocol compliance and regulatory adherence. The role involves site monitoring, staff training, data quality oversight, and documentation management in a remote position with 40-50% travel.
What they're looking for
- Bachelor's degree in life sciences or clinical research, or equivalent education and work experience
- Minimum 1 year of clinical research experience
- Detail-oriented with strong time management and organizational skills
- Excellent written and verbal communication abilities
- Proficient in Microsoft Office Suite (Word, Excel, Outlook)
- Ability to work effectively in fast-paced, changing environments
- Strong relationship-building and multitasking capabilities
What you'll be doing
- Conduct site qualification, initiation, monitoring, and closeout visits
- Monitor protocol compliance, data quality, and Good Clinical Practice requirements
- Review source documents and verify clinical study data for accuracy
- Provide training and support to investigators, coordinators, and site staff
- Manage study and regulatory documentation and prepare monitoring reports
Privacy & handoff
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