Performing site selection, initiation, monitoring and close-out visits
Supporting the development of a subject recruitment plan
Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
Collaborating with experts at study sites and with client representatives

University degree in scientific discipline or health care
At least 2 years of on-site monitoring experience
Good knowledge of clinical research regulatory requirements
Very good computer skills including MS Office
Excellent command of Spanish and English language
Organizational, time management and problem-solving skills
Ability to establish and maintain effective working relationships with coworkers, managers, and clients
Flexibility to travel
Driver’s license class B

Senior Clinical Research Associate – Sponsor Dedicated

Key skills