Clinical Research Associate 2, IQVIA
Core
Conduct independent on-site monitoring, site selection, initiation, routine visits, and closeout for clinical trials in therapeutic areas including Immunology/Gastroenterology, Dermatology, Women's Health, Asthma/Respiratory, Ophthalmology, and HIV.
Role type
Clinical Research Associate II (IC)
Builds
Clinical trial data integrity and patient enrollment
Domain
Life Sciences / Clinical Research
Deliverable
physical/clinical work
Required skills
GCP, ICH, clinical trial regulations, site monitoring, patient recruitment, query resolution, TMF management, site performance evaluation
Preferred skills
Experience in specific therapeutic areas (IM/GI, Dermatology, Women's Health, Asthma/Respiratory, Ophthalmology, HIV)
Technologies
Microsoft Office
Responsibilities
Conduct site selection, initiation, routine monitoring, and closeout visits; Build relationships with investigative sites and provide training; Monitor study progress including activation, recruitment, enrollment, and data collection; Evaluate site performance and compliance; Ensure study documentation and TMF requirements are maintained; Prepare monitoring reports; Collaborate with cross-functional teams; Support patient recruitment and retention; Assist with site financial and administrative activities.
Seniority
Mid-level, hands-on IC
