Data Analyst - PV - SME/TL/TM/SDM - PanIndia

Job Description:

Data Analyst

Joining our pharmacovigilance team, you will support Pharma companies in handling their data related to adverse effects or drugs related problems to help them stay ahead of their competition.

Your role 

As a Data Analyst, you’ll 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 (i.e. initial and follow up),
• Follow up of safety cases as per Novartis 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 prevent duplicate entries, create case (book-in) in Argus Database
• Ensure scientific rigor through accurate, complete and consistent data entry of adverse event reports 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 the essential details of the case. Self-check of online QC tool (ICSR check), case routing and case lock/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 Level Agreements (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 processing.

What you need

• A Graduate/Post Graduate/Doctorate degree in Life sciences/ Pharmacy/Medical sciences or equivalent degree
• Minimum 2 years to 6 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 team

Join us on our remarkable journey by applying right here.