Job Details
Dear Applicant,Hiring for Pharmacovigilance - TL/TM/SDMLocation - Hyderabad/Mumbai/Pune/CoimbatoreShift - GeneralNotice period - upto 2monthsRole - TM - 6-8yrs of experience in pharmacovigilance, ctc upto 18lpa SDM - 8+yrs of experience in pharmacovigilance, ctc upto 25lpaa Data Analyst, youll work on a project, with responsibility for: Triage of Safety cases Book-in and case management activities Perform Data entry of all fields including the verbatim Narrative writing / I-narrative summarizing case information for all safety cases (irrespective of report types, seriousness and versions (ie initial and follow up), Follow up of safety cases as per the process and procedures Generate action items in Argus safety data base Perform Safety case correction activities (irrespective of source, report type and seriousness) Generate action items in Argus safety data base Un-blinding (if required) Receive information on adverse events, perform initial checks, search database to preventduplicate entries, create case (book-in) in Argus Database Ensure scientific rigor through accurate, complete and consistent data entry of adverse eventreports from source documents with emphasis on timeliness and quality (full data entry) Evaluate and finish processing of expeditable/non-expeditable AE reports, including review for completeness and accuracy To perform medical coding, product coding Prepare narratives/ iNarrative summarizing theessential details of the case Self-check of online QC tool (ICSR check), case routing and caselock/closure.
Identify clinically relevant information missing from case report and facilitate its collection Perform Labelling for Serious/Non-Serious Cases and USPI labelling Work with QC Associate to improve Quality by performing self QC Attend training sessions and develop capabilities on an ongoing basis Assist with related administrative and procedural activities as required or requested Assists in the training and Mentorship of other Case Processing Associates as necessary Perform case corrections, deactivation, case rejection and NTBD (Not to be database) Responsible for completion of day-to-day work and process flows within the agreed Service LevelAgreements (SLAs) Co-ordination with team on problem solving initiatives Coordinate with internal teams to obtain necessary information required for day-today operations Consult Team Leaders, Mentor, or QC associate for any doubts related to daily case processingWhat you need A Graduate/Post Graduate/Doctorate degree in Life sciences/ Pharmacy/Medical sciences orequivalent degree Minimum 45 years to 12 years of experience in pharmacovigilance Performing Tasks consistently Self-Motivation Result Oriented Fluency in English Punctuality and Attendance Potential to work as a Team member Active Participation in developing systems and procedure in the teamInterested candidates contact HR Umme@8971074281 / [HIDDEN TEXT]