Medical Device Clinical Study Coordinator

1 week ago


Alameda, California, United States Abbott Full time

About Us

At Abbott, we are committed to helping people live more fully at all stages of life. As a global healthcare leader, our team of over 114,000 colleagues serves people in more than 160 countries.

This role offers a competitive salary range of $55,200.00-$110,400.00, commensurate with location and experience. In addition to a comprehensive compensation package, we offer a wide range of benefits, including free medical coverage for employees via our Health Investment Plan (HIP) PPO, an excellent retirement savings plan, tuition reimbursement, and education benefits.

About the Position

The Clinical Research Associate II (CRA II) will be responsible for assisting in the clinical execution and management of all aspects of assigned clinical studies. This includes planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards.

Main Responsibilities:

  • Assist in the development of study protocols and clinical study reports.
  • Conduct site visits, generate monitoring trip reports, and track resolution of action items.
  • Collaborate with cross-functional teams to evaluate and select new study investigators, and train them on study protocols and procedures.
  • Maintain and audit the Trial Master File to ensure inspection readiness.

Requirements:

  • Bachelor's degree in life sciences or equivalent with minimum 5 years of CRA or CRC experience, or combination of appropriate education and experience.
  • Must have 3+ years of relevant experience in site monitoring, clinical project management, clinical trial practices and regulations.

Benefits:

We provide a comprehensive benefits package, including free medical coverage for employees via our Health Investment Plan (HIP) PPO, an excellent retirement savings plan, tuition reimbursement, and education benefits.



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