Clinical Research Jobs at Caidya
Caidya is hiring a Clinical Research Associate I (CRA I) to support clinical trial monitoring activities in Guangzhou, China. The Clinical Research Jobs in China focus on ensuring subject safety, data integrity, and regulatory compliance while serving as the primary liaison between investigational sites and sponsors. The position offers flexibility between home- and office-based work and is ideal for early-career professionals in clinical research.
Job Details:
- Job Title: Clinical Research Associate I
- Req ID: 8254
- Location: Guangzhou, China
- Work Model: Home-based or Office-based
- Functional Area: Clinical Operations / Clinical Research
About Caidya:
Caidya is a global Clinical Research Organization (CRO) delivering specialized clinical development and monitoring services for pharmaceutical, medical device, and diagnostic studies. Operating across Asia-Pacific, Europe, and North America, Caidya supports clinical trials from study start-up to close-out.
The company works in full compliance with ICH-GCP, ISO 14155, and global regulatory standards, ensuring high-quality data, patient safety, and ethical trial conduct. Caidya is recognized for its strengths in site monitoring, regulatory support, quality management systems, and sponsor–site coordination.
With a strong focus on operational excellence, regulatory compliance, and innovation, Caidya enables efficient trial execution while supporting the professional growth of Clinical Research Associates and clinical teams worldwide.
Clinical Research Associate Role Overview:
The CRA I monitors investigational sites to ensure compliance with Caidya and sponsor SOPs, GCP/ICH guidelines, ISO 14155, and applicable regulatory requirements. The role supports clinical trial execution through site monitoring, data verification, oversight of the investigational product, and effective communication with study stakeholders.
Education & Experience for the Clinical Research Associate Role:
- Bachelor’s degree in life sciences, healthcare, or related field
- Candidates without a degree may be considered with 1+ years of relevant clinical research experience
- Less than 1 year of on-site clinical trial monitoring experience
- Experience in pharmaceutical or CRO environments is preferred
Key Responsibilities:
- In the Clinical Research Associate Role, you should conduct pre-study, site initiation, interim monitoring, and close-out visits per the Monitoring Plans
- Serve as the primary contact for assigned investigational sites
- Verify site readiness, investigator qualifications, and facility adequacy throughout the trial
- Ensure trials are conducted according to protocol, investigational plan, and regulations
- Motivate sites to meet recruitment, quality, and timeline goals in the Clinical Research Jobs in China
- Verify protection of subject rights, safety, and well-being
- Confirm informed consent is obtained prior to subject participation
- Verify enrollment of eligible subjects only
- Identify, document, and escalate protocol deviations and compliance issues
- Perform source data verification (SDV) against CRFs/EDC systems
- In the Clinical Research Associate Role, you must ensure accurate, complete, and timely data entry and query resolution
- Review and reconcile regulatory binders and essential documents
- Ensure proper documentation from study start-up through close-out
- Deliver high-quality monitoring visit reports and follow-up letters within timelines
- Perform investigational product accountability (storage, inventory, dispensing, return/destruction)
- Verify recording and reporting of adverse events and serious adverse events
- Ensure safety reporting complies with regulatory requirements and Monitoring Plans
- Support Project Teams and Clinical Operations Teams
- Participate in team meetings, training sessions, and trial-related meetings
- Support IRB/IEC and regulatory submissions when required
- Assist with feasibility assessments, monitoring tools, and study documentation
- Participate in audits and inspections as requested in the Clinical Research Jobs in China
- Work in accordance with the Caidya Quality Management System
- Identify and escalate potential fraud or misconduct per SOPs
- Accurately track time and adhere to project timelines and budgets
- Proactively manage and resolve site-related issues
- Suggest improvements to monitoring processes and workflows
Skills & Competencies Required for the Clinical Research Jobs:
- Strong understanding of GCP/ICH guidelines
- Knowledge of clinical trial processes and medical terminology
- Proficiency in Microsoft Office tools
- Good documentation and reporting skills
- Strong communication and interpersonal skills
- Attention to detail and problem-solving ability
- Effective time management and organizational skills
- Ability to work independently and in a matrix environment
- Flexibility and adaptability in a dynamic clinical research setting
- Proficiency in English
- Proficiency in the local language (reading, writing, and understanding)
Additional Requirements
- Ability to drive with a valid driver’s license (if applicable)
- Valid passport for potential international travel
- Commitment to confidentiality and ethical conduct
Why Join Caidya?
- Excellent entry point into global clinical research
- Exposure to international clinical trials and sponsors
- Flexible work arrangements (home or office-based)
- Strong focus on quality, compliance, and professional development
- Opportunity to grow within Clinical Operations and CRA career paths
