Clinical Research, Associate I

AbbVie

Alameda, California, United States
Base: $73,900.00 – $116,000.00; bonus/equity: not ...
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Ich gcp
Iso 14155
Study site visits
** AbbVie is seeking a Clinical Research Associate I to support clinical trials in Alameda, California. The role involves overseeing study data integrity, managing clinical trial processes, and ensuring compliance with regulatory standards. **

Job Summary

  • The CRA will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155.
  • Perform internal clinical studies, recruit study participants, conduct informed consent discussions with study volunteers, record study data, and maintain study files.
  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

Matching Summary

Match Score: 75

** AbbVie is seeking a Clinical Research Associate I to support clinical trials in Alameda, California. The role involves overseeing study data integrity, managing clinical trial processes, and ensuring compliance with regulatory standards. **

Salary

Base: $73,900.00 – $116,000.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • ICH GCP
  • ISO 14155
  • study site visits
  • clinical monitoring
  • trial master file

Nice-to-have

  • teamwork
  • interpersonal skills
  • communication skills
  • building rapport

Key Requirements

  • BS degree in life sciences preferred or equivalent
  • minimum 2 years of as a CRA/CRC/CTA experience
  • Experience in conducting medical device studies
  • Working knowledge of CFR
  • Proficient with Microsoft Suite

Work Rights

Not specified

Tailored Resume

Cover Letter