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| Job Location | Chennai |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | IT - Software |
| Functional Area | General / Other Software |
| EmploymentType | Full-time |
Skill required: Pharmacovigilance - Medical WritingDesignation: Management Level - New AssociateQualifications: Any GraduationYears of Experience: 0-1 yearsIn todays business environment, growth isnt just about building value-its fundamental to long-term business survival. So how do organizations sustain themselves The key is a new operating model -one thats anchored around the customer and propelled by intelligence to deliver exceptional experiences across the enterprise at speed and at scale. You will deliver breakthrough business outcomes for clients-by harnessing talent, data and intelligence to revolutionize their operating models. Operations is one of four services that make up one Accenture -the others are Strategy and Consulting, Interactive and Technology. Visit us at www.accenture.comWhat would you do You 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 :
accounts payableaccounts payablereceivableapproval processbudgetingcreditdata entryadverse eventsclinical trialsbusiness process