24 ott - Milano
Iqvia
Overview
In this role you support multicenter clinical studies by monitoring sites to ensure protocol adherence and data reporting per GCP/ICH guidelines.
You will drive site communication, training, and recruitment alignment to project needs, and manage study progress and documentation in collaboration with the study team.
The role includes ensuring TMF/ISF integrity, filtering quality issues, and possibly supporting start-up activities and site financials.
You join a global, integrity-driven organization focused on advancing patient outcomes.
Responsabilità
Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope and regulatory requirements (GCP/ICH)
Drive and track subject recruitment plans to improve predictability
Administer protocol training to sites and maintain regular communication on project expectations
Assess quality and integrity of site practices and escalate issues
Track regulatory submissions, approvals, recruitment, CRF completion, data query handling; may support start-up
Maintain Trial Master File and Investigator's Site File per GCP/ICH and local regs
Document site management activities, visit findings, and action plans; prepare visit reports and follow-up letters
Collaborate with study team for project execution; may support site recruitment plan development and invoice retrieval as applicable
Requisiti fondamentali
CRA certification according to Ministerial requirements
CRA training or prior monitoring experience
Basic knowledge of GCP/ICH regulations
Good therapeutic and protocol knowledge (training provided)
MS Office skills (Word, Excel, PowerPoint); laptop and mobile devices usage
Strong written and spoken English
Organizational and problem-solving skills
Time and financial management skills
Ability to build effective working relationships
effective communication
problem-solving
time management
GCP/ICH regulatory knowledge
site monitoring and data integrity
regulatory submissions tracking
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