Technical Writer

• May 2023 - Present

Clinical Trial Assistant

• Dec 2021 - May 2023

Key Responsibilities: • Ensure project related documentation filed in Trial Master File (TMF) in good quality and within set timelines • Handle periodic review of TMF for completeness • Handle Invoices payments procedures • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up Specialists with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines. • Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. • Assist Clinical Research Associates and Regulatory and Start-Up Specialists with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. • Accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval. • Perform assigned administrative tasks to support team members with clinical trial execution. Show less

Office Administrator

• Aug 2021 - Dec 2021