Single Sponsor CRA I / II (Must have UK monitoring exp)

Syneos Health · GBR-Remote Syneos Health is seeking a Single Sponsor CRA I / II with UK monitoring experience. As a CRA, you will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance. Responsibilities: Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits Evaluate overall performance of site and site staff, providing recommendations for site-specific actions Verify process of obtaining informed consent, protect confidentiality of subjects/patients Assess factors affecting subject/patient safety and clinical data integrity Conduct Source Document Review, verify clinical data accuracy and completeness Apply query resolution techniques, provide guidance to site staff Manage investigational product inventory, reconciliation, and storage/security Review Investigator Site File, reconcile contents with Trial Master File Document activities, support subject/patient recruitment and retention Understand project scope, budgets, and timelines; manage site-level activities May act as primary liaison with study site personnel Prepare for and attend Investigator Meetings and sponsor face-to-face meetings Provide guidance on audit readiness standards Qualifications: Bachelor's degree or RN in a related field or equivalent experience Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements Excellent communication, presentation, and interpersonal skills Ability to manage required travel of up to 75% on a regular basis