Senior Clinical Research Associate II – Medical Device Trials

Abbott

Alameda (CA)

On-site

USD 82,000 - 141,000

Full time

2 days ago
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Benefits offered by this job

Free medical coverage
High employer contribution retirement
Tuition reimbursement
FreeU education benefit

Job summary

Abbott in Alameda, CA is hiring a Clinical Research Associate II to support the clinical execution of medical device studies. You will travel to sites, perform SQV/SIV/IMV/COV visits, monitor device accountability, and help manage study timelines and regulatory compliance.

The role requires a B.S. in life sciences, 5+ years in clinical research, and 2+ years in site monitoring with ability to travel 30–50%. Strong teamwork and knowledge of GCP are essential.

Qualifications

  • B.S. degree in life sciences or equivalent, with minimum 5 years of clinical research experience.
  • 2+ years of site monitoring experience in medical device or in vitro diagnostics studies.
  • Ability to travel 30-50%.
  • Strong teamwork, communication, and problem-solving skills; knowledge of GCP and regulatory guidelines.

Responsibilities

  • Conduct single or multi-center medical device clinical studies.
  • Perform study site visits (SQV, SIV, IMV, COV) and generate monitoring reports.
  • Coordinate study start up activities and device accountability at sites.
  • Manage monitoring activities and site management per protocol and regulatory requirements.
  • Assist in planning study conduct, CRF design, and supplier/vendor selection.
  • Maintain Trial Master File and support regulatory submissions.

Education

B.S. degree in life sciences or equivalent

Tools

Microsoft Office

Job description

Abbott in Alameda, CA is hiring a Clinical Research Associate II to support the clinical execution of medical device studies. You will travel to sites, perform SQV/SIV/IMV/COV visits, monitor device accountability, and help manage study timelines and regulatory compliance.

The role requires a B.S. in life sciences, 5+ years in clinical research, and 2+ years in site monitoring with ability to travel 30–50%. Strong teamwork and knowledge of GCP are essential.

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