Clinical Data Associate II

About the role

The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed.

What you'll do

• Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner
• Conduct database build UAT and maintain quality controlled database build documentation
• Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc
• Responsible for creating, revising, appropriate versioning and maintaining data management documentation
• Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed

What you need

• 2–4 yrs of experience
• Clinical research
• PowerPoint
• SAS
• Medical coding
• Communication
• SOP writing
• Any graduate

Good to have

• SAP
• Reconciliation