Clinical Research Associate

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

Preferred

life sciences or clinical research preferred

Benefits

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.

FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

This role is based remote in the United States near a major airport or in an Abbott Office approved.

Glassdoor

3.8

Global healthcare company making diagnostics, medical devices, nutrition, and medicines.

Illinois City, Illinois, USA

https://www.abbott.com

Public Company

Total Funding

$20.01B

2026-03-09

Post Ipo Debt· $20B

2011-03-15

Post Ipo Debt· $0.1M

2009-03-16

Post Ipo Debt· $6.69M

Leadership Team

Robert Ford

Chairman & Chief Executive Officer

Jean-Yves Pavée-Callu

Senior Vice President

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Qualifications

Bachelor's 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.)

Life sciences or clinical research preferred

Minimum 1-year clinical research experience required.

Required skills

Represents the skills you have, click on the tags

Preferred skills

life sciences or clinical research preferred

Experience

1+ years