Clinical Research Associate

About the role

We are looking for a Clinical Research Associate to oversee investigator sites, ensure data quality and compliance throughout clinical trials. The role involves close interaction with site staff, principal investigators and internal teams to guarantee patient safety and timely delivery of study milestones.

Key responsibilities

• Monitor and manage investigator sites, performing source data verification and ensuring data is submitted to data management promptly.
• Identify, track and resolve issues that could affect study conduct, implementing corrective and preventive actions with site personnel.
• Train site staff on protocols, amendments and company processes, and maintain clear communication with principal investigators.
• Ensure all activities comply with ICH/GCP, local regulations and Parexel SOPs, including safety reporting and documentation.
• Maintain site documentation such as Investigator Initiation Packages, Site Master Files, and trial master file records.
• Generate monitoring reports, update corporate trial registries and provide regular progress updates after each site visit.

Required profile

• Strong interpersonal and communication skills with a flexible, quick‑learning attitude.
• Ability to work independently and manage multiple site workloads efficiently.
• Attention to detail and commitment to maintaining high data quality standards.

Required skills

• Proficiency in Chinese (spoken and written).
• Good command of written and spoken English.
• Computer literacy: word processing, spreadsheets and PowerPoint.