Senior CRA
On-siteShanghai, Shanghai, China or Beijing, Beijing, China
Job Summary
Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conduct site visits to assess performance, resolve issues, and provide support for successful trial execution. Collaborate with cross-functional teams to ensure accurate data collection and reporting while providing training and guidance to site staff. Build effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Requires approximately 60% travel. ICON is a global healthcare intelligence and clinical research organisation dedicated to bringing new medicines and treatments to patients faster.
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously
- Strong organizational and problem-solving skills
- Expertise in monitoring practices
- Data integrity expertise
- Site management expertise
- Proficiency in relevant clinical trial software and tools
- Excellent communication skills
- Interpersonal skills
- Stakeholder management skills
- Ability to influence and drive compliance within a complex environment
- Willingness to travel as required (approximately 60%)
- Legal right to work in the country where the role is based
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