Pharma Jobs at Parexel | Drug Safety Associate Post

Pharma Jobs at Parexel | Drug Safety Associate Post

Parexel Invites Pharma Candidates, Drug Safety Associate Post Vacancy. Parexel invites Candidates for the post of Drug Safety Associate. Candidates with a postgraduate degree in Pharmacy may walk in for this post on the mentioned date. Check out all the details on the same below:

Job ID 53170BR

Work Location: Bengaluru, Karnataka, India

Job Title: Drug Safety Associate

Eligibility: Degree in Pharmacy

Experience:

Associates degree in any of the above with appropriate work experience of 1-2 years in Pharmacovigilance.

Job Description:

  • Assist in the development of project specific safety procedures, workflows and templates
  • Assist in project specific safety database setup, development of data entry guidelines, and user acceptance testing
  • Triage incoming reports for completeness, legibility and validity
  • Electronic documentation and quality control of drug safety information
  • Data entry of case reports into safety database/tracking system
  • Request follow-up and perform query management
  • Coding of data in the safety database
  • Writing case narratives
  • Create and maintain project-specific working files, case report files and project central files
  • Assist with additional Drug Safety Specialist on activities as required
  • Inform Line Manager (LM)/Team Manager, Safety Services Project Leader (SSPL) or Project Leader (PL) and Regional Head of PV Operations of potential change-in-scope of projects
  • Support of Medical Directors/Safety Physicians, as needed, in medical monitoring activities
  • Participate in client and investigator meetings as required
  • Attend internal, drug safety and project specific training sessions
  • Perform literature searches
  • Preparation for, participation in, and follow up on audits and inspections
  • Delegate work as appropriate to Drug Safety Assistants
  • Assistance in development of Expedited Reporting Procedures
  • Assistance with registration with relevant authorities for electronic reporting on behalf of the sponsor
  • Assistance with setting up and deployment of worldwide reporting as required to regulatory authorities, CECs, local ECs, and investigator sites (electronic and hard copy)
    Submission of safety reports to investigators via ISIS (International Safety Information System)
  • Assist with measuring investigative site performance in conducting required tasks in ISIS
    Tracking and filing of submission cases as required
  • Assist with unblinding of SUSARs, as required
  • Support collection and review of metrics for measuring reporting compliance
  • Support Global Pharmacovigilance Information Office (GPIO) in the collection and organization of global PV requirements
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