Clinical Data Coordinator II- North Wales, PA

The selected candidates will review Case Report Form (CRF) data for completeness, accuracy and consistency; identify and resolve data discrepancies; as appropriate, apply level corrections to CRFs; generate and resolve (as appropriate) data queries; update/correct/review data in the clinical databases based on resolved data queries; perform data listings review; update tracking systems as necessary; create and maintain study files and appropriate study documentation.

In addition to the above responsibilities, the Clinical Data Coordinator II may also assist with database testing, SSP preparation & review and other data management activities e.g. medical dictionary coding, SAE reconciliation, external data reconciliation, and effectively mentor less experienced staff (may include assisting and guiding new personnel during their initial training period).

The qualified candidate should possess a degree in the life sciences or equivalent clinical data work experience. Accuracy and attention to detail is essential. Knowledge of medical terminology is a plus. A minimum of one year of relevant Clinical Data Management experience required.

ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity.