Site selection, initiation, monitoring, and close-out
Recruitment plan development and tracking
IQVIA Inc is seeking a Clinical Research Associate for oncology or immunology, responsible for ensuring compliance with protocols and regulations at study sites. The role includes site monitoring, recruitment management, quality assurance, and mentoring clinical staff, requiring at least 2.5 years of relevant experience and strong organizational skills
Job Summary
Conduct selection, initiation, monitoring, and close-out visits in line with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Collaborate with sites to develop, drive, and track recruitment plans, enhancing predictability and meeting project needs.
Provide protocol training and maintain regular communication with sites to manage expectations and address issues.
Matching Summary
Match Score: 85
IQVIA Inc is seeking a Clinical Research Associate for oncology or immunology, responsible for ensuring compliance with protocols and regulations at study sites. The role includes site monitoring, recruitment management, quality assurance, and mentoring clinical staff, requiring at least 2.5 years of relevant experience and strong organizational skills.
Salary
Base: $69,800.00 - $226,800.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Health and welfare and/or other benefits may be offered
Skills & Requirements
Must-have
GCP and ICH guidelines adherence
Site selection, initiation, monitoring, and close-out
Recruitment plan development and tracking
Protocol training and site communication
Trial Master File (TMF) and Investigator's Site File (ISF) documentation