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. #J-18808-Ljbffr

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