Senior Clinical Research Associate
On-site · Guangzhou, Guangdong, China or Wuhan, Hubei, China
Job Summary
Senior Clinical Research Associate at ICON plc accountable for leading clinical trial monitoring activities with emphasis on quality and continuous improvement. Responsibilities include monitoring sites for protocol and GCP compliance, conducting site visits, collaborating with cross-functional teams for timely data collection and reporting, training site staff and other CRAs, and building strong relationships with site personnel to ensure smooth trial operations. Requires strong independent work capabilities, travel around 60%, and a bachelor’s degree in a related field. ICON offers a comprehensive benefits package and a diverse, inclusive work environment.
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills
- Willingness to travel as required (approximately 60%)
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