QC Reviewer

Our client is looking for “QC Reviewer” with strong expertise in “Clinical Trials” and “Clinical Knowledge”

Job Description-

• The successful candidate will have the ability to integrate information from the clinical database to ensure high quality data that enables appropriate analyses for successful regulatory submissions of oncology compounds. 

• The candidate would review and modify submission-ready clinical documents by demonstrating high attention to detail, in order to guarantee quality of the final document. 

• The ability to work independently to think through results, resolve data discrepancies, be able to comb through long data dense documents, analyze, interpret and apply new clinical data with a focus on the key messages is essential.

• Ability to review data across multiple documents for consistency. 

• The candidate must be able to actively participate in cross-functional clinical teams and provide deliverables according to timelines. 

Most Critical Skills: 

• Review docs against source; Cross-Tracking.

• Clinical knowledge of Oncology.

The candidate should expect a phone interview first, then if chosen for a f2f interview they should expect 2-3 interviews, plus a test that will be 1-1.5 hours in duration. CIA SCREENING PRIOR TO START.