Job Title:
CRA I (Clinical Research Associate I)
Location:
Beijing, China – Client Site
Job ID:
25102057
Company Overview:
Syneos Health® is a fully integrated biopharmaceutical solutions organization that accelerates customer success by translating clinical, medical affairs, and commercial insights into outcomes.
Highlights:
Patient- and customer-centric clinical development model
Agile, innovative team environment
29,000 employees across 110 countries
Inclusive Total Self culture fostering authenticity and belonging
Job Summary:
The CRA I conducts on-site and remote monitoring of clinical research studies to ensure compliance with GCP and regulatory standards. This role develops monitoring tools, tracks study progress, and contributes to the implementation of processes and policies to ensure high-quality trial conduct.
Key Responsibilities:
Conduct on-site and remote monitoring of clinical studies
Review study protocols, informed consent forms (ICFs), and case report forms (CRFs) for compliance
Develop and implement monitoring tools, procedures, and processes (e.g., monitoring plans, checklists, templates)
Participate in the design, implementation, and delivery of SOPs, processes, and training materials
Manage defined project components, including site visits, study tracking, and issue resolution
Document monitoring activities accurately (monitoring reports, follow-up letters, action plans)
Collaborate with investigators, site staff, and cross-functional teams to ensure smooth study execution
Qualifications:
Bachelor’s degree in a related field or equivalent experience
2–4 years of clinical research monitoring experience
Strong 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 clinical trial management systems and relevant software
Preferred Certifications:
Certified Clinical Research Associate (CCRA) or equivalent
Necessary Skills:
Attention to detail and strong analytical skills
Problem-solving and critical thinking
Team collaboration skills
Strong organizational and time management skills
Proficiency in Microsoft Office Suite
Impact and Contribution:
Ensures adherence to clinical practices and regulatory requirements, contributing to the quality and integrity of studies
Supports the development of monitoring tools and procedures to enhance trial efficiency
Plays a key role in advancing medical knowledge and improving patient outcomes
Job Category:
Clinical Operations / Clinical Monitoring / CRA
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