Clinical Research Coordinator

Responsibilities

• You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits
• 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

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

• 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
• Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants
• Strong written and verbal communication skills, with attention to detail and time management
• Comfortable using CTMS, eCRFs, and Microsoft Office tools
• Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants.

Required skills

• CTMS, Clinical Research, Clinical Site Operations, Drug Development, ECRFs, Electrocardiography (ECG), Laboratory Specimen Processing, Phlebotomy, Vital Signs Measurement

Experience

• 1+ years