Accenture Released Job Openings On 01/10/2021.Accenture is a leading global professional services company, providing a broad range of services in strategy and consulting, interactive, technology and operations, with digital capabilities across all of these services..Application form link provided at the end of post.Â
Vacancy Details:
Accenture Recruiting B.Pharma,M.Pharma Candidates with 03 – 05 years of Experience for Pharmacovigilance – Medical Writing Position.Complete Details for the Pharmacovigilance – Medical Writing as follows.
Important Details :
- Location :Chennai
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 01/10/2021
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Job Description/Skills Required
- 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.
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