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Clinical Research Associate

Abbott

Remote · USResearch$61–123K/yrSeen 1w agoSeen in employer's feed 2 days ago

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At a glance

Compensation
$61–123K/yr
Location
Remote · US
Role Type
Research
Work Authorization
Not specified

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Job overview

Abbott’s Core Lab business unit is hiring a Clinical Research Associate to support clinical trial sites from study start-up through closeout. The role is remote in the United States near a major airport or in an approved Abbott office. Reporting to the Clinical Manager, the associate works with clinical project teams and operations leadership in a regulated quality environment, managing assigned tasks and timelines under general supervision.

Skills & qualifications

RequiredNice to have

Skills

Attention to DetailTime ManagementWritten CommunicationVerbal CommunicationOrganizationPresentation SkillsCollaborationSelf-DirectionMultitaskingPrioritizationComputer SkillsMicrosoft Office Suite

Qualifications

Bachelor's or Equivalent Education and Experience1+ Years Clinical Research Experience

Benefits

Medical Insurance
401(k) Match
Tuition Assistance

Full job description

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:

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/ (http://www.abbottbenefits.com/pages/candidate.aspx)

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.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email [email protected]

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