Job Description

Title: Clinical Research Associate (CRA) - B

Location: San Diego, CA

Duration: 8 Months

100% Onsite

RESPONSIBILITIES:

• Carry out assigned functions applying knowledge and skill in an accurate, timely manner.
• Apply knowledge of FDA regulations to site monitoring and clinical study design duties.
• Monitor and maintain necessary supplies, with approval by senior department staff.
• Maintain effective, professional, timely, and consistent communications with clinical sites both in person, and via all available correspondence media (telephone, email, web, etc.)
• Support and/or lead clinical research study start up activities (includes creation of study protocols, clinical study reports, regulatory binders, study logs, work instructions, case report form, and other study related materials)
• Ability to train site personnel on study activities including investigational product usage, maintenance and accountability, sample collection, testing and shipping, data entry and query resolution
• Study monitoring (includes assessing the familiarity of the site personnel with the protocol, procedures and investigational product, assessing protocol compliance and investigational product accountability as applicable, source document verification, identifying protocol deviations, writing queries, writing monitoring reports, notes to file, and other documentation as necessary)
• Independent site management skills to assist with study problem identification and solving, and ensure timely study progression
• Understanding of clinical research activities including tasks associated with study start up, interim monitoring, close out, data collection and central files
• Team player able to deliver on project timelines.
• Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices; build productive internal/external working relationships
• Other duties as assigned, according to the changing needs of the business.

Consultants Eligible Benefits Upon Waiting Period:

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account (for High-Deductible Health Plans)
• Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
• Supplemental Life Insurance
• Short Term Disability (coverage varies by state)
• Long Term Disability
• Critical Illness, Hospital coverage, Accident Insurance
• MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
• 401(k)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.

Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.

• Published on 02 Apr 2026, 7:29 PM

Job Tags

Full time, Temporary work, Interim role, Flexible hours

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