Embark on your clinical research journey with VitalBio as an Entry-Level Clinical Trials Associate. Ensure studies are organized and compliant through meticulous documentation management.
As a vital member of VitalBio's clinical operations team, you will support preclinical and clinical trials by managing essential documentation workflows. This role is perfect for early-career life sciences professionals with a robust grasp of ICH-GCP guidelines. Your ability to communicate effectively and maintain audit-ready documentation will keep studies on track.
Key Responsibilities:
• Maintain accurate CTMF/eTMF per company SOPs
• Conduct routine reviews of study files for completeness
• Archive important regulatory documents efficiently
• Reconcile documentation gaps prior to audits
• Update trackers for enrollment and critical study milestones
Requirements:
• Bachelor’s degree in life sciences or a related field
• 0-2 years of experience in clinical research preferred
• Advanced skills in eTMF platforms and Microsoft Excel
• Strong knowledge of ICH-GCP guidelines
• Familiarity with EDC tools like Medrio is a plus
Leverage your organizational skills and attention to detail in a role that supports healthcare innovation at VitalBio.
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