Clinical Research Associate II (Latvia) - Remote, Sponsor-Dedicated

About the role

Syneos Health is hiring a remote, sponsor-dedicated Clinical Research Associate II (CRA II) for Latvia. The role covers site qualification, initiation, interim monitoring, site management and close-out, performed on-site or remotely, and ensures regulatory, ICH-GCP and protocol compliance. For Real World Late Phase studies, the title used is Site Management Associate II.

Key responsibilities

• Perform site qualification, initiation, interim monitoring, site management and close-out visits, evaluating site performance and escalating serious issues
• 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, labelling and release, and reconcile the Investigator Site File with the Trial Master File
• Support recruitment and retention, enter tracking data, and prepare sites for audits
• Attend investigator and sponsor meetings, clinical training and global project meetings
• For Real World Late Phase: site support throughout the study lifecycle, chart abstraction, data collection and collaboration with sponsor affiliates, medical science liaisons and local country staff

Required profile

• Bachelor's degree or RN in a related field, or equivalent education, training and experience
• Good computer skills and willingness to adopt new technologies
• Excellent communication, presentation and interpersonal skills
• Ability to travel regularly up to 75%

Required skills

• Knowledge of Good Clinical Practice (ICH-GCP) and other applicable regulatory requirements
• Working knowledge of ICH/GCP guidelines, regulations and company SOPs