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Drug Safety Specialist

GlobalChannelManagementInc

Marlborough, MA, United States contract

Posted: June 7, 2017

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Quick Summary

A Drug Safety Specialist with 5-7 years of experience in Cognos report development and project management, preferably within the pharmaceutical industry, is required to join our team.

Job Description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation.  Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function.  Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.

Drug Safety Specialist  needs 5-7 years in Cognos report development and project management, preferably within the pharmaceutical industry.

Drug Safety Specialist requires:

• Pharmacovigilance, project management
• Experience working with validated applications is preferred.
• Understanding
of Oracle business applications and reporting tools is essential,
including web-based and client-server applications running in an Oracle
Argus, Internet/Intranet, Cognos environment.
• Familiarity with Crystal Reports, SAS and Empirica preferred.
• working knowledge of CFR Part 11 is essential.
• Familiarity with ICH and GxP guidance and regulations.

Drug Safety Specialist duties are:

• Be
able to create advanced level reports utilizing Cognos, SQL, Argus
reporting, Adobe Acrobat, MS Excel and other tools as needed for
aggregate reporting, safety data surveillance, data mining and risk
management. 30%

• Manage IM internal and external projects
and vendors. Setup projects plans, ensure adherence to timelines.
Contribute at team, cross-functional, external and vendor meetings on
specifications gathering, project plans, request. 30%

• Be
experienced in Pharmacovigilance safety data processing and Oracle's
Adverse Event Reporting System (Argus) or other similar application for
the tracking of drug safety data to contribute to decisions for report
design and testing of system configurations. 20%

 

• Support
in documentation, testing and validation of reports and functionality
of Argus and Cognos. Contribute to process improvement and SOP and WI
writing.20%

$80/hr

6  months

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