Clinical Research Associate 2, IQVIA

IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The Clinical Research Associate II conducts independent on-site monitoring activities, supports investigative sites, tracks study progress and compliance, maintains trial documentation, and collaborates with cross-functional teams to deliver clinical studies successfully.

Responsibilities

Conduct site selection, initiation, routine monitoring, and closeout visits in accordance with GCP, ICH, and applicable regulatory requirements

Build strong relationships with investigative sites and provide protocol, process, and study-specific training

Monitor study progress, including site activation, patient recruitment, enrollment, data collection, and query resolution

Evaluate site performance and compliance, identifying risks and escalating quality concerns when appropriate

Ensure study documentation, regulatory records, and Trial Master File (TMF) requirements are maintained accurately and are inspection-ready

Prepare monitoring reports, follow-up communications, and other required study documentation

Collaborate with cross-functional study teams to support successful project delivery and achieve study milestones

Support patient recruitment and retention initiatives at the site level

Assist with site financial and administrative activities, including invoice management, when applicable

Benefits

Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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

• Bachelor's degree required
• Minimum 1 year of independent on-site monitoring experience in a CRO, biotech or pharmaceutical
• Working knowledge of GCP, ICH, and clinical trial regulations
• Strong communication, organizational, and problem-solving skills
• Proficiency with Microsoft Office applications

Required skills

Independent On-Site Monitoring, Clinical Practice (GCP), ICH Guidelines, Clinical Trial Regulations, Microsoft Office, Central Nervous System (CNS) Clinical Research, Cardiovascular Clinical Research, Obesity Clinical Research, MASH/NASH Clinical Research

Experience

1+ years