Remote Clinical Research Associate – Core Lab

Abbott; United States; Remote; USD 61,000 - 123,000; Full time

Benefits offered by this job

Health insurance

401(k) retirement plan

Tuition reimbursement

Education benefits

Job summary

Abbott is a global healthcare leader offering opportunities across diagnostics, medical devices, nutritionals and branded medicines. The Clinical Research Associate role is remote in the United States near a major airport or in an Abbott Office with approval.

As a CRA, you’ll support clinical trial sites from start-up to closeout, ensuring studies meet protocols, regulatory requirements, and company procedures. Travel is significant and collaboration with cross-functional teams is essential.

Qualifications

• Bachelor’s degree in life sciences or equivalent combination of education and work experience.
• Minimum 1 year clinical research experience required.
• Detail-oriented with strong time management and organizational skills.
• Excellent written and verbal communication; ability to work with others in a fast-paced, changing environment.

Responsibilities

• Conduct site qualification, initiation, monitoring, and closeout visits.
• Provide training and support to investigators, study coordinators, and site staff.
• Monitor protocol compliance, data quality and GCP requirements.
• Review source documents and verify study data for accuracy and completeness.
• Ensure eligible participants are enrolled and manage regulatory documentation.
• Monitor investigational product accountability and inventory.
• Prepare monitoring reports and communicate findings and actions.

Skills

Communication

Time management

Attention to detail

Team collaboration

Multitasking

MS Office

Education

Bachelor’s in Life Sciences

Tools

Microsoft Office

Job description

Abbott is a global healthcare leader offering opportunities across diagnostics, medical devices, nutritionals and branded medicines. The Clinical Research Associate role is remote in the United States near a major airport or in an Abbott Office with approval.

As a CRA, you’ll support clinical trial sites from start-up to closeout, ensuring studies meet protocols, regulatory requirements, and company procedures. Travel is significant and collaboration with cross-functional teams is essential.