Senior Clinical Research Associate 1 - Sponsor Dedicated
IQVIA UK
Barcelona, Spain
Site selection and monitoring
Gcp and ich guidelines
Regulatory submission tracking
Perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan
Job Summary
Perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan.
Evaluate the quality and integrity of site practices in accordance with regulatory requirements, managing progress by tracking submissions, recruitment, CRF completion, and data query resolution.
Enjoy the stability and resources of a leading global contract research organization while gaining direct experience with one of our customers, with access to world-class training and mentoring.
Matching Summary
Perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan.
Skills & Requirements
Must-have
site selection and monitoring
GCP and ICH guidelines
regulatory submission tracking
case report form completion
data query resolution
Nice-to-have
human data science company
flexible work schedules
career growth resources
diverse perspectives valued
Key Requirements
At least 2 years of on-site monitoring experience
University degree in scientific discipline or health care