Advance your clinical research career as a Clinical Operations Associate at VitalBio. This role focuses on maintaining compliance with ICH-GCP guidelines and managing essential document workflows efficiently. VitalBio seeks detail-oriented specialists for a pivotal role in clinical operations as it transitions into Preclinical and Clinical trials.

You'll manage the Clinical Trial Master File (CTMF) and support site staff with data accuracy, enhancing collaboration and communication. This position is ideal for candidates with a foundational understanding of clinical research practices and a proactive approach to problem-solving. Key Responsibilities:
Maintain CTMF/eTMF following ICH-GCP and SOPs
Review study files and site documents for completeness




Collect and archive essential regulatory documents
Reconcile documentation gaps before audits
Update study trackers for patient enrollment Requirements:
Bachelor's degree in life sciences or related field
0–2 years clinical research experience preferred
Proficiency in eTMF platforms and Microsoft Excel
Familiarity with ICH-GCP guidelines
Experience with EDC tools is a plus Bring your detail-oriented mindset and commitment to VitalBio’s mission of transforming healthcare.

📌 Clinical Operations Associate At Vitalbio Oakville (Canada)
🏢 Vital Bio
📍 Canada