Senior Clinical Research Associate 1 - Sponsor Dedicated
IQVIA
Barcelona, Spain
Site selection, initiation, monitoring, close-out
Subject recruitment plan evaluation
Gcp and ich guidelines adherence
Perform site selection, initiation, monitoring and close-out visits, support the development of a subject recruitment plan, and evaluate the quality and integrity of site practices
Job Summary
Perform site selection, initiation, monitoring and close-out visits, support the development of a subject recruitment plan, and evaluate the quality and integrity of site practices.
Manage progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution, while collaborating with experts at study sites and client representatives.
Enjoy the stability and resources of a leading global contract research organization with access to world-class training and mentoring in an environment designed to help you gain experience in a wide variety of therapeutic areas.
Matching Summary
Perform site selection, initiation, monitoring and close-out visits, support the development of a subject recruitment plan, and evaluate the quality and integrity of site practices.
Skills & Requirements
Must-have
site selection, initiation, monitoring, close-out
subject recruitment plan evaluation
GCP and ICH guidelines adherence
tracking regulatory submissions
computer skills including MS Office
excellent command of Spanish and English
Nice-to-have
human data science company
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
Organizational, time management and problem-solving skills
Ability to establish and maintain effective working relationships