CRA II Multi-Sponsor (Remote)

About the role

Syneos Health is hiring a CRA II for a multi-sponsor clinical study, working remotely. The role covers site qualification, initiation, interim monitoring, site management and close-out, ensuring regulatory, ICH-GCP and protocol compliance. For Real World Late Phase studies, the title used is Site Management Associate II, with added responsibilities such as chart abstraction and site support throughout the study lifecycle.

Key responsibilities

• Perform site qualification, initiation, interim monitoring, site management and close-out visits, on-site or remotely, and escalate serious issues to the project team
• Verify informed consent, protect subject confidentiality and assess factors affecting safety and data integrity
• Review source documents and CRFs, resolve queries and verify electronic data capture compliance
• Check investigational product inventory, dispensing and administration, and ensure proper labelling, import and release
• Review the Investigator Site File and reconcile it with the Trial Master File
• Document activities, support recruitment and retention, enter data into tracking systems and manage site-level communication
• Act as liaison with site personnel, prepare for and attend investigator and sponsor meetings, and support audit readiness
• For Real World Late Phase: support sites from identification to close-out, abstract charts, collect data, and suggest potential sites based on local knowledge

Required profile

• Bachelor's degree or RN in a related field, or equivalent education, training and experience
• Knowledge of Good Clinical Practice/ICH guidelines and other regulatory requirements
• Good computer skills and willingness to adopt new technologies
• Excellent communication, presentation and interpersonal skills
• Ability to travel regularly up to 75%