Data Specialist

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

**Job Description**

Provides compliance support to the clinical trial process by ensuring all study documentation and source data is captured accurately in eCRF, up to date and first time right. Performs quality reviews and answers any eCRF queries in a timely manner. Reviews accuracy of the Investigator Site Files (ISF) as well as performs quality compliance checks and answering any CRF queries in a timely manner

**Day to day responsibilities:**

+ Act as the primary point of contact for sponsors representative.
+ Maintains ISF and study trackers as delegated and ensures that ICFs are correctly completed.
+ Completes data capturing activities on one or more studies across multiple sites and regions.
+ Ensures accurate and timely entry of all data in the eCRF from the source notes and tracks the flow of the eCRFs and queries.
+ Verifies prot...