Experienced clinical research associate, iqvia biotech

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7hvrv1

Experteer Overview As a Clinical Research Associate, you will oversee site monitoring to ensure study conduct and data reporting align with protocol, GCP, ICH, and sponsor requirements. You will coordinate with sites, manage recruitment plans, and train site staff to uphold project expectations. You'll assess site quality, elevate issues, and track regulatory submissions, enrollment, and data queries. You'll maintain TMF/ISF documentation and support cross‐functional project execution. This role offers exposure to hands‐on trial management and the chance to contribute to high‐quality clinical research. Responsibilities Perform site monitoring visits (selection, initiation, monitoring and close‐out) per scope and regulatory guidelines Drive, adapt and track subject recruitment plans to meet project needs Administer protocol training and maintain regular site communication to manage expectations Evaluate site practices for protocol conduct and regulatory compliance; evaluate quality issues Track regulatory submissions, approvals,



recruitment/enrollment, CRF completion/submission, and data queries; may support start‐up Ensure TMF/ISF documentation is complete and compliant Create documentation on site management, visit findings and action plans; submit visit reports and follow‐up letters Collaborate with study team for project execution support Support development of site recruitment plans and, if applicable, site financial management Qualifications University Bachelor's Degree and Master's Degree in scientific discipline or health care CRA Certification as required by regulatory decree Experience in pharma industry or clinical trials Strong computer skills (MS Office) and excellent English Organizational, time management and problem‐solving skills Ability to establish effective working relationships and travel flexibility Driver's license class B #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7hvrv1