Clinical Research Associate II (FSP) – Xi'an

The role involves monitoring and managing investigator sites for clinical trials, ensuring data quality, compliance, and effective communication with healthcare professionals. It is suitable for candidates with clinical monitoring experience and a background in life sciences or related fields.

Location: China

Responsibilities

• Conducts source data verification (SDV) and ensures timely data submission.
• Identifies and resolves issues impacting study conduct.
• Manages investigator site workload efficiently.
• Ensures studies comply with ICH/GCP, local laws, and SOPs.
• Maintains patient safety and reports safety issues.
• Informs and collaborates with Principal Investigator and site staff.
• Develops corrective and preventative actions.
• Handles all aspects of site management from selection to closeout.
• Trains site staff on protocols and processes.
• Understands product, protocol, and therapy area.
• Interacts professionally with healthcare providers.

Requirements

• At least 1.5 years (preferably 2 years) of clinical monitoring/site management experience.
• Good knowledge of ICH/GCP and relevant regulations.
• Proficient in Chinese and English.
• Good interpersonal and communication skills.
• Flexible, quick learner, able to manage multiple tasks.