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Drug Safety Specialist

Marlborough, MA, United StatesRemoteContract

AI Summary

Contract Drug Safety Specialist responsible for creating advanced reports for pharmacovigilance, managing projects and vendors, and supporting documentation and validation of Argus and Cognos systems.

About this role

Drug Safety Specialist

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.


Qualifications

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%




Additional Information

$80/hr

6 months

Skills

Adobe AcrobatArgus ReportingCFR-Part 11CognosICHMS ExcelOraclePharmacovigilanceProject ManagementSQL

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