CRA II - Beijing
On-site · Beijing, Beijing, China
Job Summary
On-site and remote monitoring of clinical research studies with a focus on ensuring compliance with clinical practices. Develop and implement monitoring tools, procedures, and processes (monitoring plans, checklists, templates); contribute to SOPs and training materials; coordinate site visits and track study progress; produce monitoring reports, follow-up letters, and action plans; collaborate with investigators, site staff, and stakeholders to ensure smooth study conduct. Requires a Bachelor's degree (or equivalent experience) and 2-4 years in clinical research monitoring, strong knowledge of GCP/regulatory requirements, excellent communication, ability to work independently, and proficiency with clinical trial management systems; CCRA or equivalent certification preferred. The role emphasizes attention to detail, problem-solving, teamwork, and strong organizational skills in a global, cross-functional environment.
Required Qualifications
- Bachelor's degree in a related field or equivalent experience
- Minimum of 2-4 years of experience in clinical research monitoring
- Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
- Excellent communication and interpersonal skills
- Ability to work independently and manage multiple priorities
- Proficiency in using clinical trial management systems and other relevant software
- Certifications: Certified Clinical Research Associate (CCRA) or equivalent certification preferred
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