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Job Location | Bangalore |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | IT - Software |
Functional Area | General / Other Software |
EmploymentType | Full-time |
Skill required: Pharmacovigilance - Medical WritingDesignation: Senior AnalystQualifications: Master of PharmacyYears of Experience: 5-8 yearsYou will be aligned with our Pharmaceuticals Processes vertical and help us with the processes to collect, monitor, research, assess and evaluate information on the adverse effects of medication with a view to identifying new information about hazards associated with medicines and consequently, prevent harm to patients. It also deals with the reviewing and resolving of discrepancies identified by the system or through manual checks as per guidelines. Employees under this span can also be responsible for a number of activities related to the design, development, and maintenance of Clinical Database objects.You will be working as a part of Pharmacovigilance team which designs and maintains a safety database to monitor single case support activities; source distribution for business partners and perform medical literature searches. Responsible for data entry, MedDRA coding, and label assessment of the adverse events in SUSAR cases. If there are issues with the provided information, the scientist is contacted for verification.A medical editor (or scientific editor) revises scientific language for usage, flow, and clarity. It is about reducing awkward phrasing, biased language, and jargon that is inappropriate for the audience. You will provide support for clinical submission narrative writing for Phase 1-4 clinical trials in accordance with client SOP. Narratives are required to be written based on data listings and/or safety reports.What are we looking for We are looking for individuals who have the following skillset:
Keyskills :
customer relationsreportingbasisaccountsresearchdata entryadverse eventsclinical trialsnarrative writingmeddra codingvisitdealsdesignmanualmeddracheckstrialsmedical