Clinical Research Associate I — On-Site Trials (Alameda)

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

Benefits offered by this job

HIP PPO medical plan

Retirement savings plan

Tuition reimbursement

FreeU education benefit

Job summary

Abbott in Alameda, California is seeking a Clinical Research Associate I to ensure data quality and integrity across multiple trials. The role is on-site and requires travel up to 30-50% with management support for study startup, monitoring, and regulatory activities.

The candidate should have a life sciences degree and at least one year of clinical research experience, with familiarity in GCP/ CFR guidelines and regulatory affairs. Abbott offers strong benefits and career growth opportunities.

Qualifications

• BS degree in life sciences with minimum one year of clinical research experience.
• Experience with CFR/ICH-GCP and regulatory affairs is preferred.
• Excellent teamwork and strong interpersonal and communication skills.
• Proficiency with Microsoft Office tools and related software.

Responsibilities

• Perform study site visits (SQV, SIV, IMV, COV) and generate monitoring reports.
• Assist with clinical monitoring and site management to ensure regulatory compliance.
• Support study startup activities and shipping of study devices to sites.
• Maintain and audit Trial Master File (TMF) and upload to eTMF for inspection readiness.
• Contribute to planning, CRF design, and training of study sites.
• Communicate study status to management and assist in regulatory submissions.

Skills

Teamwork

Interpersonal skills

Communication skills

GCP knowledge

Microsoft Suite

Education

BS degree in life sciences

Tools

eTMF system

Job description

Abbott in Alameda, California is seeking a Clinical Research Associate I to ensure data quality and integrity across multiple trials. The role is on-site and requires travel up to 30-50% with management support for study startup, monitoring, and regulatory activities.

The candidate should have a life sciences degree and at least one year of clinical research experience, with familiarity in GCP/ CFR guidelines and regulatory affairs. Abbott offers strong benefits and career growth opportunities.