Clinical Research Associate

Abbott; California; Remote; USD 61,000 - 123,000; Full time

Benefits offered by this job

HIP PPO medical plan

Excellent retirement plan

Tuition reimbursement

FreeU education benefit

Fortune-recognized workplace

Job summary

Abbott is seeking a Clinical Research Associate to support sites in the United States from a remote or Abbott Office location. You will oversee site qualification, initiation, monitoring, and closeout while ensuring compliance with protocols and regulatory standards.

The role reports to Clinical Manager and collaborates with Clinical Project Teams. Travel up to 40% and a fast-paced, regulated environment are expected.

Qualifications

• Bachelor's degree in life sciences or clinical research (or equivalent).
• Minimum 1 year clinical research experience.
• Detail-oriented with strong time management.
• Excellent written and verbal communication skills.
• Able to work collaboratively in a fast-paced environment.
• Travel: 40%.

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.
• Review source documents and verify study data for accuracy.
• Ensure eligible participants are enrolled.
• Maintain study and regulatory documentation.
• Monitor investigational product accountability and inventory.
• Review adverse event reporting for accuracy and compliance.
• Assess site performance including recruitment and retention.
• Prepare monitoring reports and communicate findings and corrective actions.
• Build relationships with sites and internal stakeholders.
• Develop knowledge of applicable clinical research regulations and study types.

Skills

Clinical trial monitoring

Regulatory compliance

Documentation

Cross-functional collaboration

Communication skills

Time management

Education

Bachelor's degree (life sciences or clinical research)

Equivalent work experience

Tools

Microsoft Office

Regulatory databases

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:

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 and on Facebook at

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 an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day), Driving a personal auto or company car or truck, or a powered piece of material handling equipment, Keyboard use (greater or equal to 50% of the workday), Lift, carry, push or pull weights of more than 20 pounds/9 kilos on a regular/daily basis, Work with human blood or other potentially infectious materials, Work with infectious organisms or known infectious materials

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. EEO is the Law link - English: is the Law link - Espanol: