Clinical Research Intern

This is a fully remote position, open to applicants in United States.

📋 Description

• Ensure the maintenance and updating of study information on ClinicalTrials.gov, guaranteeing accuracy and adherence to regulatory standards.

• Conduct document filing, tracking, and management within Veeva Vault, making sure all study documents are up-to-date, complete, and ready for audits.

• Provide assistance with Electronic Data Capture (EDC) data management tasks and user additions.

• Aid in data entry and verification processes for the TLC study, ensuring a high level of accuracy and promptness.

• Support the maintenance of site data within the BSI Clinical Trial Management System (CTMS), including updating site details and monitoring site status.

• Assist with quality assurance checks and reconciliation across clinical systems to ensure the consistency of study data.

• Work collaboratively with members of the Clinical team to facilitate study start-up, ongoing maintenance, and close-out activities as needed.

• Follow Standard Operating Procedures (SOPs), ICH-GCP guidelines, and relevant regulatory requirements in all assigned tasks.

⛳️ Requirements

• Currently enrolled in a degree program in sciences, healthcare, or a related discipline.

• Exceptional attention to detail and strong organizational abilities.

• Competence in Microsoft Office Suite (Excel, Word, Outlook).

• Capable of managing multiple tasks simultaneously while meeting set deadlines.

• Excellent communication and teamwork capabilities.

• A genuine interest in clinical research and regulatory affairs.

🏝️ Benefits

• Opportunity to gain hands-on experience in clinical research.

• Exposure to regulatory processes and industry standards.

• Collaborative work environment with experienced professionals.