Clinical Research Associate, Early Clinical Development

Responsibilities

Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines

Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals

Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues

Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity

Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries

Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards

Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence

Work closely with cross-functional project teams to support study execution and ensure alignment with project goals

Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking

Benefits

Depending on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered.

Depending on the position offered, a range of health and welfare and/or other benefits may be offered.

Glassdoor

3.9

IQVIA provides analytics, compliance, and management solutions to the life sciences industry.

Durham, North Carolina, USA

https://www.iqvia.com

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Education and Training

Engineering and Development

Management and Executive

Sales

Customer Service and Support

Product Management

Marketing

Accounting and Finance

Creatives and Design

Arts and Entertainment

Trends of Total Sponsorships

*2026

(150)

2025

(163)

2024

(282)

2023

(255)

2022

(229)

Qualifications

Bachelor's degree in life sciences or health-related field (or equivalent experience)

Requires at least 1.5 years of on-site monitoring experience

Strong understanding of GCP, ICH guidelines, and regulatory requirements

Requires at least 1.5 years of on-site monitoring experience.

Required skills

Clinical Site Monitoring, Clinical Practice (GCP), ICH Guidelines, Regulatory Compliance

Experience

1+ years