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As a Clinical Research Associate, you will support the initiation, on-site and remote monitoring, and close-out of clinical trial sites, ensuring participant safety, data integrity, and compliance with ICH-GCP, SOPs, and regulatory requirements.
Job Responsibility:
Monitor clinical trials on-site and remotely in line with TFS/sponsor SOPs, ICH-GCP, and regulations
Ensure subject safety, protocol adherence, informed consent compliance, and data accuracy
Review source documentation and CRFs and verify Investigational Product management
Document monitoring activities in timely, accurate reports and escalate issues when needed
Maintain ISF and deliver required documents to TMF/eTMF
update CTMS and project systems
Support audits, inspections, and clinical supply management (as applicable)
Requirements:
Bachelor’s degree in life sciences, nursing, or equivalent
1+ year of relevant clinical experience
Solid understanding of medical terminology, GCP, ICH guidelines, and regulatory requirements
Strong communication, organization, and time-management skills
tech-savvy and detail-oriented
Ability to work independently and collaboratively in a matrix team environment
Fluent in English
flexible, proactive, analytical, and collaborative mindset
What we offer:
competitive compensation package
comprehensive benefits
opportunity for personal and professional growth in a rewarding environment
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