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Clinical Research Associate I

Abbott · Alameda, CA

RoleLantern checked active
Clinical OperationsFull-time$74k–$116kCompany career page

RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.

Role summary

Abbott seeks a Clinical Research Associate to ensure data quality and regulatory compliance across clinical trials in Alameda, California. Responsibilities include coordinating study activities, conducting site visits, managing trial documentation, and supporting regulatory submissions. A life sciences degree with 0–1 year of clinical research experience is preferred, with medical device or diagnostics study background advantageous.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-05 (originally posted 2026-08-19). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

  • Bachelor's degree in life sciences or equivalent combination of education and experience
  • 0-1 year CRA/CRC/CTA experience or 2+ years relevant clinical experience
  • Medical device and/or in-vitro diagnostics study experience preferred
  • Working knowledge of CFR, ICH-GCP, and clinical regulatory affairs
  • Strong teamwork, interpersonal, and communication skills
  • Proficiency with Microsoft Office Suite
  • Phlebotomy certification preferred

What you'll be doing

  • Conduct internal clinical studies, recruit participants, perform informed consent, and maintain study documentation
  • Execute site visits, generate monitoring reports, and track resolution of action items
  • Ensure protocol compliance and adherence to GCP guidelines, ICH standards, and federal regulations
  • Maintain and audit Trial Master File and upload to eTMF system for inspection readiness
  • Review clinical data for completeness and accuracy; escalate issues to management

Privacy & handoff

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What RoleLantern checked

RoleLantern compiled this listing from the employer's public posting. We check that the application link is live and how recently the role appeared — the employer has not submitted or confirmed it on RoleLantern.

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Date posted48 days ago
Last source checkToday
Salary listedListed
Location clearClear
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