Clinical Research Associate I

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

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.

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

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.

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