Clinical Research Associate I

Abbott

Alameda, California, United States
Base: $73,900.00 – $116,000.00; bonus/equity: not ...
Onsite
Bs degree in life sciences or equivalent
Minimum one year clinical research experience
Working knowledge of cfr and ich-gcp
Abbott is seeking a Clinical Research Associate I to join their team in Alameda, California. The role focuses on ensuring the quality and integrity of clinical trial data while offering significant career development and a supportive work environment

Job Summary

  • The Clinical Research Associate ensures quality, accuracy, and integrity of clinical trial data throughout the full lifecycle according to federal regulations and GCP guidelines.
  • Abbott offers comprehensive benefits including free medical coverage, a high employer contribution retirement plan, and tuition reimbursement programs.
  • This onsite role in Alameda, CA requires performing study site visits, generating monitoring reports, and maintaining inspection-ready Trial Master Files.

Matching Summary

Match Score: 85

Abbott is seeking a Clinical Research Associate I to join their team in Alameda, California. The role focuses on ensuring the quality and integrity of clinical trial data while offering significant career development and a supportive work environment.

Salary

Base: $73,900.00 – $116,000.00; Bonus/Equity: Not specified; Benefits: Competitive compensation, incentives, 401(k) match, medical/dental/vision

Skills & Requirements

Must-have

  • BS degree in life sciences or equivalent
  • Minimum one year clinical research experience
  • Working knowledge of CFR and ICH-GCP
  • Proficiency with Microsoft Suite
  • Ability to travel 30-50% of the time

Nice-to-have

  • Experience with medical device studies
  • Background in in-vitro diagnostics
  • Pharmaceutical industry background
  • Strong interpersonal and communication skills
  • Teamwork excellence and rapport building

Key Requirements

  • BS degree in life sciences preferred
  • Minimum one year clinical research experience
  • Knowledge of CFR, ICH-GCP, and ISO14155
  • Microsoft Suite proficiency required
  • Willingness to travel up to 50%

Work Rights

Not specified

Tailored Resume

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