Remote Clinical Research Associate: Trials & Compliance

Thornton Tomasetti; California; Hybrid; USD 61,000 - 123,000; Full time

Benefits offered by this job

Free medical coverage

Retirement plan

Tuition reimbursement

Education benefit

Job summary

Abbott is seeking a Clinical Research Associate to support site monitoring from start-up through closeout, ensuring compliance with protocols and regulatory requirements. The role partners with Clinical Project Teams and Operations, working in a regulated quality environment to meet study timelines.

Based remotely in the United States near a major airport or at an Abbott office, travel is up to 40%. The position requires at least 1 year of clinical research experience and strong communication

Qualifications

• Bachelor's degree in life sciences or clinical research; related experience acceptable.

Responsibilities

• Support clinical trial sites from study start-up through closeout.
• Ensure studies are conducted in compliance with protocols and regulatory requirements.
• Collaborate with Clinical Project Teams and Operations leadership to drive study success.
• Prepare monitoring reports and communicate findings, risks, and corrective actions.

Skills

Attention to detail

Time management

Communication skills

Team collaboration

Self-directed

Multitasking

Microsoft Office

Education

Bachelor's degree in life sciences or clinical research

Tools

Microsoft Office Suite

Job description

Abbott is seeking a Clinical Research Associate to support site monitoring from start-up through closeout, ensuring compliance with protocols and regulatory requirements. The role partners with Clinical Project Teams and Operations, working in a regulated quality environment to meet study timelines.

Based remotely in the United States near a major airport or at an Abbott office, travel is up to 40%. The position requires at least 1 year of clinical research experience and strong communication