Clinical Study Assistant
posted by: spj_bot
Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
The Clinical Trial Assistant (CTA) supports the planning and execution of Phase 1/2 clinical trials across multiple countries by providing operational, administrative, and logistical assistance. Working closely with the Project Director and clinical study leaders, the CTA helps ensure smooth study coordination, high-quality documentation, and effective communication with CROs and external vendors in a fast-paced biotech setting, and reports directly to the Project Director.
Main Responsibilities:
- Supports daily clinical trial execution and logistics
- Organizes team meetings and cross-functional coordination
- Maintains Trial Master File (TMF) quality and completeness
- Manages essential study and regulatory documents
- Supports study start-up and vendor/CRO coordination
- Assists with contracts, work orders, and purchase orders
- Ensures effective communication and tracks key updates/decisions
Requirements