Launch your career in clinical operations with VitalBio as a Clinical Trials Associate. You will manage essential documentation and support studies in a highly organized, detail-oriented environment.
VitalBio is seeking a Clinical Trials Associate to enhance its creative preclinical and clinical trial efforts. This entry-level role requires a strong understanding of ICH-GCP guidelines and excellent communication skills. You will maintain the CTMF/eTMF, conduct review processes, and act as a key resource for site staff.
Key Responsibilities:
• Maintain CTMF/eTMF to ICH-GCP guidelines and SOPs
• Review study files for accuracy and completeness
• Archive essential regulatory documents like IRB approvals
• Reconcile documentation gaps before audits




• Update study trackers for patient enrollment and milestones
Requirements:
• Bachelor’s degree in life sciences or related field
• 0-2 years in clinical research (IVD, CRO, Pharma preferred)
• Proficiency in eTMF platforms and advanced Excel skills
• Familiarity with ICH-GCP guidelines and workflows
• Experience with EDC tools like Medrio preferred
Bring your organizational skills and attention to detail to VitalBio's transformative clinical research team.
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📌 Clinical Trials Associate at VitalBio (Oakville)
🏢 Jaide Health
📍 Oakville