Document Management Associate

About the role

This role will be responsible for the overall management and quality maintenance of essential clinical trial and other designated documents, including the set up and maintenance of the Trial Master File (TMF) The CDS will have a strong focus on ensuring routine document management operations are performed with adherence to Novotech SOPs.

What you'll do

• CDS will perform the responsibilities of the SDMA (refer to job description) to the highest competency and act as both a document uploader and QC reviewer
• CDS is responsible to liaise directly with the client/alliance partner counterpart (if assigned) with respect to assigned responsibilities
• CDS will contribute to maintenance and delivery of team Training Programs and serve as a trainer/mentor to new team members
• Identify, develop and lead potential TMF process improvements which can improve centralised workflows and drive efficiencies across Novotech
• May undertake line management responsibilities of the DMA team as required to assist the Clinical Operations Management team

What you need

• 5–9 yrs of experience
• Clinical research
• SOP writing
• CRO
• Any graduate