Clinical Research, Associate I

jobs.abbott

Alameda, California, United States
Base: $73,900.00 – $116,000.00; bonus/equity: not ...
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Clinical trial data management
Clinical study coordination
Regulatory compliance monitoring
** Abbott is seeking a Clinical Research Associate I to support clinical trials in its Alameda, California location. Ideal candidates will have a background in life sciences with clinical research experience, ensuring data integrity and compliance with regulatory standards. **

Job Summary

  • Abbott is a global healthcare leader that helps people live more fully at all stages of life with a portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines.
  • The Clinical Research Associate I will perform internal clinical studies, coordinate study activities, conduct site visits, and ensure compliance with regulatory and company standards.
  • Employees have access to career development, excellent medical coverage, retirement plans, tuition reimbursement, and a diverse and inclusive workplace recognized globally.

Matching Summary

Match Score: 75

** Abbott is seeking a Clinical Research Associate I to support clinical trials in its Alameda, California location. Ideal candidates will have a background in life sciences with clinical research experience, ensuring data integrity and compliance with regulatory standards. **

Salary

Base: $73,900.00 – $116,000.00; Bonus/Equity: Not specified; Benefits: Medical coverage, retirement savings plan, tuition reimbursement

Skills & Requirements

Must-have

  • clinical trial data management
  • clinical study coordination
  • regulatory compliance monitoring
  • Good Clinical Practices (GCP)
  • clinical site visits and monitoring
  • Microsoft Suite proficiency

Nice-to-have

  • teamwork and interpersonal skills
  • experience with medical device studies
  • knowledge of CFR and ICH guidelines
  • communication with clinical management
  • study device accountability

Key Requirements

  • BS degree in life sciences or equivalent
  • minimum 2 years CRA/CRC/CTA experience
  • experience in medical device or in-vitro diagnostics studies preferred
  • working knowledge of CFR, ICH-GCP, and regulatory affairs

Work Rights

Not specified

Tailored Resume

Cover Letter