Clinical Research Associate

Abbott (abbottcareers2 board); United States; Remote; USD 61,000 - 123,000; Full time

Job summary

Abbott is seeking a Clinical Research Associate (CRA) to support sites from start-up through closeout. The role requires working in a regulated, quality-focused environment and collaborating with Clinical Project Teams and Operations.

The candidate will monitor sites for protocol compliance, data quality, and GCP, while managing timelines and regulatory documentation. Remote work in the United States is allowed near airports or Abbott offices, with up to 50% travel.

Qualifications

• Bachelor's (life sciences or clinical research preferred) or equivalent combination of education and work experience.
• Minimum 1-year clinical research experience.
• Detail-oriented with strong time management.
• Excellent written and verbal communication; well organized.

Responsibilities

• Support clinical trial sites from study start-up to closeout.
• Ensure studies comply with protocols, regulatory requirements, and company procedures.
• Build cross-functional relationships with Clinical Project Teams and Operations.
• Monitor data quality and GCP compliance; review source documents.

Skills

Attention to detail

Time management

Communication skills

Team collaboration

Self-directed

Multitasking

Microsoft Office

Education

Bachelor's degree or equivalent in life sciences/clinical research

Tools

Microsoft Office Suite

Job description

JOB DESCRIPTION:

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life.

You'll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with a high employer contribution.
• Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity:

Our Core Lab business unit currently has an opportunity for a Clinical Research Associate. This role is based remote in the United States near a major airport or in an Abbott Office approved.

Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments, and informatics systems is often the first step in patient care decision-making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.

What You'll Work On:

As a Clinical Research Associate (CRA), you will support clinical trial sites from study start-up through closeout, ensuring studies are conducted in compliance with protocols, regulatory requirements, and company procedures.

This role reports to the Clinical Manager and partners with Clinical Project Teams and Operations leadership. The successful candidate will work in a regulated quality environment, manage assigned tasks and timelines, build cross-functional relationships, and contribute to study success under general supervision.

Key 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.

Required Qualifications

• Bachelor's (life sciences or clinical research preferred) or equivalent combination of education and work experience.
• Minimum 1-year clinical research experience required.
• Must be detail-oriented and efficient in time management.
• Must have excellent written and verbal communication, organizational and presentation skills.
• Must be able to work effectively with others.
• Self-directed and able to work within a fast paced and constantly changing environment.
• Ability to multitask, prioritize, and manage time efficiently.
• Proficient computer skills, including Microsoft Office Suite (Word, Excel, Outlook, etc.).
• Travel: 40 %

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: https://abbottbenefits.com/

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at abbott.com , on LinkedIn at https://www.linkedin.com/company/abbott-/ , and on Facebook at https://www.facebook.com/AbbottCareers .

The base pay for this position is $61,300.00 - $122,700.00 In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Medical & Scientific Affairs

DIVISION:

CRLB Core Lab

LOCATION:

United States > California : Remote

ADDITIONAL LOCATIONS:

United States of America : Remote

WORK SHIFT:

Standard

TRAVEL:

Yes, 50 % of the Time

MEDICAL SURVEILLANCE:

Yes

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in