Maintain and update study information on ClinicalTrials.gov, ensuring accuracy and compliance with regulatory requirements
Perform document filing, tracking, and maintenance within Veeva Vault, ensuring all study documents are current, complete, and audit-ready
Assist with EDC (Electronic Data Capture) data management activities and adding users
Assist with data entry and data verification activities for the TLC study, ensuring high level of accuracy and timeliness
Support site data maintenance in the BSI CTMS, including updating site information and tracking site status
Assist with quality checks and reconciliation across clinical systems to ensure consistency of study data
Collaborate with Clinical team members to support study start-up, maintenance, and close-out activities as needed
Adhere to SOPs, ICH-GCP guidelines, and applicable regulatory requirements in all assigned

Clinical Research Intern

Key skills