Clinical Research Associate (CRA) – Level 2

About the role

IQVIA Biotech is seeking a Clinical Research Associate (CRA) Level 2 to support on‑site monitoring of clinical trials in oncology, cardiovascular or internal medicine. The role ensures compliance with protocols, regulatory standards and sponsor expectations.

Key responsibilities

• Conduct site visits—including selection, initiation, monitoring, and close‑out—following GCP and ICH guidelines.
• Collaborate with site staff on subject recruitment strategies and track enrollment progress.
• Provide protocol‑specific training to site personnel and maintain ongoing communication.
• Assess site performance, document findings, and escalate quality concerns as needed.
• Maintain essential documents in the Trial Master File (TMF) and Investigator Site File (ISF) according to regulatory standards.

Required profile

• Bachelor’s degree in life sciences or a related health field, or equivalent experience.
• Minimum of 1 year of on‑site monitoring experience.
• Ability to travel as required by project needs.

Required skills

• Strong understanding of Good Clinical Practice (GCP).
• Familiarity with ICH guidelines and regulatory requirements.
• Experience with site management activities and documentation.