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 strong 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
- Robust 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.