Associate I Clinical Research
$73.9k - $116kAbbott
Abbott seeks a Clinical Research Associate to ensure quality and integrity of clinical trial data across multiple studies in medical devices. The role involves site visits, monitoring activities, regulatory compliance, and data management in an onsite position in Alameda, California.
Responsibilities
- Conduct site visits and generate monitoring reports; track action item resolution
- Perform clinical monitoring and ensure protocol compliance with GCP and regulatory requirements
- Manage study device accountability, reconciliation, and supply logistics
- Maintain Trial Master Files and upload to eTMF for inspection readiness
- Review clinical data for completeness and accuracy; escalate issues to management
Requirements
- Bachelor's degree in life sciences or equivalent education
- Minimum one year of clinical research experience
- Knowledge of CFR, ICH-GCP, and clinical regulatory affairs
- Proficiency with Microsoft Office Suite
- Strong teamwork and interpersonal communication skills
- Medical device or in-vitro diagnostics study experience preferred
Vacancy posted 2 days ago
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