Clinical Research Associate 2, IQVIA

IQVIA•Durham, NC
•$74,500 - $197,500•Onsite

About The Position

IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team. We are looking for professionals with experience in one or more of the following therapeutic areas: Central Nervous System (CNS), Cardiovascular, Obesity, MASH/NASH. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Requirements

  • 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.

Nice To Haves

  • Experience in Central Nervous System (CNS)
  • Experience in Cardiovascular
  • Experience in Obesity
  • Experience in MASH/NASH

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

  • health and welfare and/or other benefits
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service