QC Reviewer

QC Reviewer

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

This is Direct Hire with our Client

Job Description

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.

Qualifications

EDUCATION AND PRIOR EXPERIENCE:

• BS/MS degree with 3+ year experience with clinical trials and clinical knowledge.

• Must have a good understanding of principles of clinical research as well as clinical trial operations.

• Experience with study and data management issues related to healthy volunteer and patient studies is desired. Hands-on experience with software programs such as MS Excel, MS Word, PowerPoint.

• A superior command of the English language and grammar, excellent oral and written communication skills as well as demonstrated knowledge of clinical and the ability to work effectively with people and lead teams is essential.

• MT/CLS license beneficial.