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| Job Location | Bangalore |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | IT - Software |
| Functional Area | Bio Tech / R&D / Scientist |
| EmploymentType | Full-time |
Skill required: Pharmacovigilance - Medical AffairsDesignation: AssociateJob Location: BengaluruQualifications: Bachelor of Dental Surgery/Bachelor of Pharmacy/Master of PharmacyYears of Experience: 1-3 yearsAbout Accenture OperationsIn 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.In Medical Affairs, you will have to design, develop and deliver business solutions related to the medical affairs group of pharmaceutical companies, including thought leadership development, medical publications, education and information, medical grants, advisory boards and advocacy, regulatory review and approval of pharmaceutical drugs and perform publishing and quality control tasks on submission components.What are we looking for We are looking for individuals who have the following skillset:
Keyskills :
data entryadverse eventsquality controlmedical affairsadvisory boardsbusiness processbusiness solutionsthought leadershipdigital conversionstatements of work sow