Clinical Research Associate I – Alameda (Onsite)

Abbott; Alameda (CA); On-site; USD 74,000 - 116,000; Full time

Benefits offered by this job

HIP PPO medical plan

Retirement savings plan with high-emlo

Tuition reimbursement

FreeU education benefit

Equal Opportunity Employer

Job summary

Abbott in Alameda, California is seeking a Clinical Research Associate I to ensure quality and integrity of clinical trial data across multiple studies according to CFR, ICH GCP, and ISO14155. This is an on-site role in Alameda, not remote.

You will perform site visits, assist monitoring, manage TMF, support study start-up, and coordinate with RA/QA during audits. Must have a BS in life sciences and at least one year of clinical research experience; travel up to 50%.

Qualifications

• BS degree in life sciences preferred or equivalent with minimum one year of clinical research experience.
• Experience working on medical device studies and/or in vitro diagnostics preferred.
• Demonstrate excellence in teamwork and communication with team members and management.

Responsibilities

• Perform study site visits (SQV, SIV, IMV, COV) and generate monitoring reports.
• Assist clinical monitoring and site management, ensuring protocol and GCP compliance.
• Participate in study start-up activities and shipping of study devices to sites.
• Maintain Trial Master File (TMF) and upload to eTMF to ensure inspection readiness.
• Review clinical data listings for completeness and accuracy; communicate with management.

Skills

Clinical monitoring

Regulatory knowledge

Study coordination

Teamwork

Education

BS in life sciences

Tools

Microsoft Suite

Job description

Abbott in Alameda, California is seeking a Clinical Research Associate I to ensure quality and integrity of clinical trial data across multiple studies according to CFR, ICH GCP, and ISO14155. This is an on-site role in Alameda, not remote.

You will perform site visits, assist monitoring, manage TMF, support study start-up, and coordinate with RA/QA during audits. Must have a BS in life sciences and at least one year of clinical research experience; travel up to 50%.