Clinical Research Associate

IQVIA

. Perform site monitoring visits, including selection, initiation, monitoring, and close-out visits .

Posted 11/9/2026full-timeUnited StatesJuniorMid-Level💰 $74,500 - $175,100 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial site management, including monitoring visits, regulatory compliance, and effective communication with study sites. Proficient in managing project execution and recruitment plans while adhering to GCP and ICH guidelines.

Highest-signal resume keywords

Clinical Trial Site ManagementRegulatory Compliance (GCP/ICH)Site Monitoring VisitsProject ExecutionSubject Recruitment Plans

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Research Regulatory RequirementsProtocol KnowledgeData Query GenerationTrial Master File ManagementCRF CompletionSite Finances ManagementMonitoring Documentation MaintenanceProblem-Solving SkillsTime Management SkillsOrganizational Skills

Soft Skills

Written Communication SkillsVerbal Communication SkillsInterpersonal Skills

Tools & Technologies

Microsoft WordMicrosoft ExcelMicrosoft PowerPointLaptop ComputerIPhoneIPad

Certifications & Qualifications

CRA Training Program (Preferred)

Industry Keywords

Clinical ResearchSite MonitoringSubject RecruitmentRegulatory AdherenceStudy Training

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Perform site monitoring visits, including selection, initiation, monitoring, and close-out visits
Work with sites to adapt, drive, and track subject recruitment plans
Administer protocol and study training to assigned sites
Establish regular communication with sites to manage project expectations and issues
Evaluate study site practices for protocol quality, integrity, and regulatory adherence
Escalate quality issues as appropriate
Track regulatory submissions and approvals, recruitment and enrollment, CRF completion and submission, and data query generation and resolution
Support the study start-up phase when applicable
Ensure site documents are available for Trial Master File filing
Verify Investigator's Site File maintenance according to GCP/ICH and local regulatory requirements
Maintain site management and monitoring documentation, visit reports, follow-up letters, and other study documents
Collaborate with study team members to support project execution
Support development of project subject recruitment plans on a per-site basis when applicable
Manage site finances according to clinical trial agreements and retrieve invoices when applicable

Requirements

What you’ll need

Bachelor's Degree in scientific discipline or health care preferred; requirement indicated
Equivalent combination of education, training and experience may be accepted in lieu of degree
Some organizations require completion of CRA training program or prior monitoring experience
Basic knowledge of applicable clinical research regulatory requirements, including GCP and ICH guidelines
Good therapeutic and protocol knowledge as provided in company training
Proficiency in Microsoft Word, Excel, and PowerPoint
Ability to use a laptop computer, iPhone, and iPad where applicable
Written and verbal communication skills, including good command of English
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 and welfare benefits
Incentive plans, bonuses, and/or other forms of compensation may be offered