Senior Clinical Data Associate

About the role

The Senior Clinical Data Associate 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
• Assist in developing CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders
• Conduct database build UAT and maintain quality controlled database build documentation. May oversee overall quality of the clinical database
• 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

What you need

• 5–9 yrs of experience
• Clinical research
• SOP writing
• PowerPoint
• Medical coding
• SAS
• Clinical data management
• Any graduate

Good to have

• SAP
• Reconciliation