Leyden Labs

General

• Assist the Clinical Trial Teams in ensuring the most effective and efficient conduct of clinical trials by providing administrative and project tracking support
• Support the preparation, handling, distribution, collection and archiving of clinical study documents and reports, including contracts and invoices
• Ensure that all study files are periodically reviewed for completeness and maintained in accordance with Good Clinical Practices, applicable regulations and company procedures
• Interface with internal colleagues and external vendors and partners
• Work closely with the Clinical Operations Team to support the effective execution of clinical studies and maintain high standards of quality and compliance

Senior Clinical Trial Associate