Clinical Research Associate – Sponsor Dedicated

IQVIA

. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required .

Posted 4/28/2026full-timeParsippany • Kansas, New Jersey, North Carolina • 🇺🇸 United StatesJuniorMid-Level💰 $71,900 - $189,000 per yearWebsite

About the role

Key responsibilities & impact

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work
Work with sites to adapt, drive, and track subject recruitment plans
Administer protocol and related study training to assigned sites
Evaluate the quality and integrity of study site practices
Manage the progress of assigned studies by tracking regulatory submissions and approvals
Ensure copies/originals (as required) site documents are available for filing
Create and maintain appropriate documentation regarding site management
Collaborate and liaise with study team members for project execution support

Requirements

What you’ll need

Bachelor's Degree in scientific discipline or health care preferred
Requires at least 1 year of on-site monitoring experience
Equivalent combination of education, training and experience may be accepted in lieu of degree
Good knowledge of applicable clinical research regulatory requirements
Good therapeutic and protocol knowledge as provided in company training
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
Written and verbal communication skills including good command of English language
Organizational and problem-solving skills
Effective time and financial management skills
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Benefits

Comp & perks

Health insurance
Retirement plans
Paid time off
Flexible work arrangements
Professional development opportunities
Bonuses

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

on-site monitoringstudy data reportingsubject recruitment plansprotocol administrationregulatory submissionsstudy documentationclinical research regulatory requirementstherapeutic knowledgeprotocol knowledge

Soft Skills

written communicationverbal communicationorganizational skillsproblem-solving skillstime managementfinancial managementrelationship building