CRA II: Medical Device Clinical Trials Specialist

Abbott; Alameda (CA); On-site; USD 82,000 - 141,000; Full time

Benefits offered by this job

Free medical coverage in HIP PPO plan

High employer retirement contribution

Tuition reimbursement

FreeU education benefit

Diversity recognition

Job summary

Abbott, based in Alameda, CA, is seeking a Clinical Research Associate II to support the execution and management of assigned clinical studies for medical devices and diagnostics.

You will plan, monitor, and collaborate with sites to meet timelines and quality standards, including site visits, study startup activities, device accountability, data reviews, and regulatory submissions. Travel 30–50% required.

Qualifications

• BS in life sciences or equivalent with minimum 5 years of clinical research experience.
• 2+ years of site monitoring experience.
• Experience in medical device and/or in-vitro diagnostics studies preferred.
• Must be able to travel 30–50%.

Responsibilities

• Conduct single or multi-center medical device clinical studies.
• Perform study site visits (SQV, SIV, IMV, COV) and monitor action items.
• Participate in study startup activities and device accountability.
• Maintain and audit Trial Master File and assist in regulatory submissions.
• Communicate status of studies to management and ensure on-time delivery.

Skills

Clinical research

Site monitoring

GCP knowledge

Study coordination

Education

B.S. in life sciences

Tools

Microsoft Suite

Job description

Abbott, based in Alameda, CA, is seeking a Clinical Research Associate II to support the execution and management of assigned clinical studies for medical devices and diagnostics.

You will plan, monitor, and collaborate with sites to meet timelines and quality standards, including site visits, study startup activities, device accountability, data reviews, and regulatory submissions. Travel 30–50% required.