Clinical Research Coordinator, On-Site

IQVIA is a leading global provider of clinical research services, and they are seeking a Clinical Research Coordinator to join Avacare. The role involves managing clinical trials, overseeing patient recruitment, and ensuring compliance with regulatory standards.

Responsibilities

• Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish
• Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training

Company

• Clinical research, commercial insights, and healthcare intelligence for life sciences.
• Durham, North Carolina, USA
• https://www.iqvia.com/
• Founded in 1982
• 10001+ employees

Qualifications

• Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens
• Solid understanding of site operations and the drug development process
• Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants for CRC I
• Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants for CRC II
• Strong written and verbal communication skills, with attention to detail and time management
• Comfortable using CTMS, eCRFs, and Microsoft Office tools
• Glassdoor
• 3.9
• IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
• Durham, North Carolina, USA
• https://www.iqvia.com
• H1B Sponsorship
• Data Powered by
• Distribution of Different Job Fields Receiving Sponsorship
• Represents job field similar to this job
• Management and Executive
• Engineering and Development
• Sales
• Customer Service and Support
• Product Management
• Education and Training
• Marketing
• Accounting and Finance
• Creatives and Design
• Arts and Entertainment
• Trends of Total Sponsorships
• *2026
• (150)
• 2025
• (163)
• 2024
• (282)
• 2023
• (255)
• 2022
• (229)
• 2021
• (208)
• 2020

Required skills

• CTMS, Clinical research, Clinical trial management, Drug development process, ECG, Lab specimen processing, Microsoft Office, Phlebotomy, Site operations, eCRFs

Experience

• 1-3 years