Friday, January 22, 2010

Data Analyst in Rochester, NY

Friday, January 22, 2010
Our client is looking to hire a Data Analyst on a full time basis.

Experience:
Working knowledge of relational database (Required).
Microsoft Access - Access SQL (Required)
Customer Service (Required)
Visual Basic/VBA (Preferred)
SAS (Preferred)
Crystal Reports (Preferred)
TSQL (Preferred)
SQL Server 2005 programming (Preferred)
Clinical Trials Data Management (Preferred)

Experience: 1. Assist in the setup of Clinical Trials protocols - includes test setup, requisitions and patient reports design. If required, custom programming relating to special protocol flagging.
2. Communicate and participate in teleconferences with sponsors and CROs about data file specifications and data transmission schedules
3. Responsible in developing data file requirements, Data Management Agreement, with the Sponsor/CRO.
4. Work with the Programmers and/or Management in designing and developing a data extraction program based on the requirements in the Data Management Agreement.
5. Responsible for the setup, documentation (Interlab Agreement), coordinating and QC of external laboratories (partner and reference labs) data transfers.
6. Responsible for the documentation (Process Notes) and validation of the data extraction program.
7. Perform regular QC checks on protocol data and monitoring the data imports into the Clinical Trials Repository.
8. Coordinate data transfers, data reconciliation and database locking activities with the CRO/Sponsor Data Management Group.
9. If required, responsible for implementing any protocol setup changes for active trials.
10. If required, develop protocol specific adhoc or custom reports.
11. Responsible for the archiving of protocol data as outlined in the Standard Operating Procedures (SOP).
12. Provide back up coverage in Reporting department during periods of PTO or absences for the Reporting staff.
13. Performs duties with a general working knowledge of FDA, NYSDOH, GCP, ICH, and other pertinent regulations, as pertains to central laboratory functions.
14. Understands and follows company policies and procedures while always maintaining patient confidentiality, both inside and outside of the work place.


**All candiates must be US Citizen or GC Holder**
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