Associate Clinical Data Manager - RTSM

The Senior Clinical Research Associate (SCRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. This role would suit a SCRA who has had exposure to Lead responsibilities and wanting to take a step up into site management. 

This single sponsor (FSP) role will be based from our Melbourne or Sydney office and we offer hybrid working arrangements and full flexibility in working hours to ensure our staff achieve the work-life balance often missing in this role. 

The CRA is the primary contact between the Investigational Sites, Novotech and Sponsor. Key responsibility of a CRA is as a site relationship manager ensuring that clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs.

Responsibilities:

• CRAs primary responsibility...