Clinical Research, Associate I

Abbott

Alameda, California, United States
Base: $73,900.00 – $116,000.00; bonus/equity: not ...
Ensure quality, accuracy and integrity of clinical trial data
Perform internal clinical studies
Conduct informed consent discussions
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

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.
  • Abbott is a global healthcare leader that helps people live more fully at all stages of life.

Matching 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.

Salary

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

Skills & Requirements

Must-have

  • ensure quality, accuracy and integrity of clinical trial data
  • perform internal clinical studies
  • conduct informed consent discussions
  • perform study site visits
  • assist and conduct clinical monitoring
  • maintain and audit Trial Master File (TMF)

Nice-to-have

  • excellence in teamwork
  • solid interpersonal and communication skills
  • flexibility in daily activities

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 and/or in-vitro diagnostics studies preferred
  • Working knowledge of CFR, ICH-GCP

Work Rights

Not specified

Tailored Resume

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