Senior Clinical Research Associate 1 - Sponsor Dedicated
IQVIA
Multiple Locations
Site selection and monitoring
Gcp and ich guidelines
Regulatory submissions tracking
Perform site selection, initiation, monitoring and close-out visits, and manage progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution
Job Summary
Perform site selection, initiation, monitoring and close-out visits, and manage progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.
Gain experience in a wide variety of therapeutic areas with access to world-class training and mentoring.
Enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
Matching Summary
Perform site selection, initiation, monitoring and close-out visits, and manage progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.
Skills & Requirements
Must-have
site selection and monitoring
GCP and ICH guidelines
regulatory submissions tracking
computer skills including MS Office
Spanish and English language proficiency
Nice-to-have
career growth resources
flexible work schedules
therapeutic knowledge building
better work-life balance
diversity and inclusion culture
Key Requirements
University degree in scientific discipline or health care
At least 2 years of on-site monitoring experience
Good knowledge of clinical research regulatory requirements