Clinical Research Associate

Abbott • Lake Forest, CA

3d • Remote

About The Position

Abbott’s Core Lab business unit is hiring a Clinical Research Associate (CRA) to support clinical trial sites from study start-up through closeout. The role is remote in the United States near a major airport or at an approved Abbott office. The CRA works in a regulated quality environment to help ensure studies comply with protocols, regulatory requirements, and company procedures. The position reports to the Clinical Manager and partners with Clinical Project Teams and Operations leadership. The successful candidate manages assigned tasks and timelines, builds cross-functional relationships, and contributes to study success under general supervision. Travel is required; the posting lists both 40% and 50% of the time.

Requirements

• Bachelor’s degree or equivalent combination of education and work experience.
• At least 1 year of clinical research experience.
• Detail-oriented with efficient time management.
• Excellent written and verbal communication, organizational, and presentation skills.
• Ability to work effectively with others.
• Self-directed and able to work in a fast-paced, constantly changing environment.
• Ability to multitask, prioritize, and manage time efficiently.
• Proficient computer skills, including Microsoft Office Suite (Word, Excel, Outlook, etc.).

Nice To Haves

• Bachelor’s degree in life sciences or clinical research preferred.

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 Good Clinical Practice (GCP) requirements.
• Review source documents and verify clinical study data for accuracy and completeness.
• Ensure only eligible participants are enrolled in studies.
• Manage and maintain study and regulatory documentation.
• Monitor investigational product accountability and inventory.
• Review adverse event reporting for accuracy and compliance.
• Assess site performance, including patient recruitment and retention efforts.
• Prepare monitoring reports and communicate findings, risks, and corrective actions.
• Build strong relationships with clinical research sites and internal stakeholders.
• Develop knowledge of applicable clinical research regulations and study types.

Benefits

• Career development opportunities with an international company.
• Employees can qualify for free medical coverage in the Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• Retirement savings plan with a high employer contribution.
• Tuition reimbursement.
• Freedom 2 Save student debt program.
• FreeU education benefit, providing an affordable and convenient path to a bachelor’s degree.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level