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 innovative preclinical and clinical trial efforts.

This entry-level role requires a robust 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.

📌 Clinical Trials Associate at VitalBio (Oakville)
🏢 Jaide Health
📍 Oakville