Job title: Medical Reviewer – PanIndia
Company: Advika Solutions
Job description: Job Description: Medical Reviewer we’re creating a culture that enables exceptional outcomes. Forget business as usual. This is about pursuing some of the world’s most exciting, cutting-edge technologies inspired solutions that enhance the lives of
Job Description: Medical Reviewer we’re creating a culture that enables exceptional outcomes. Forget business as usual. This is about pursuing some of the world’s most exciting, cutting-edge technologies inspired solutions that enhance the lives of millions across the globe. Our workplace thrives on ideas and opportunities. Everyone is invited to challenge convention, and this role is no exception. Join us as Medical Reviewer, drive the next gen innovations in Life Sciences. Your role As a Medical Reviewer, you’ll work on a variety of projects, with responsibility for: Online and offline Medical Review of safety reports in Argus Core and through line listing. Review and validation/amendment of product coding. Review/amendment of narrative for its appropriateness as per Novartis narrative writing conventions Review and validation/amendment of event selection, coding (as per MedDRA current version), grouping/ linking and event ordering. Review and validation/amendment of seriousness criteria (as per applicable WP) Support medical function for the assigned activities Review and confirmation/amendment of Expectedness / Listedness / Labeling of the event Determination and addition of causality (as per applicable WP) Providing Medical Assessment Comment (MAC), where applicable (as per applicable WP). Requesting for relevant follow-up information Action item generation Certain countries non serious cases have to be reviewed Responding to medical queries raised by the case processors and QC (Quality Control) associate and provide feedbacks to them Reporting to Team leader/Team manager on performance, status and any escalations Provide triage support for medical judgement related queries. Participating in product safety meetings Responsible to conduct Best practice sessions amongst team for quality improvement. What you need A Graduate/Post-Graduate/Doctorate degree in medical sciences or equivalent degree (MBBS/MD) Minimum 2 years of experience in medical review of ICSR or minimum 1 year of experience in aggregate analysis. Self-motivation Personal grooming and etiquette Inter-personal effectiveness Achievement orientation Relationship building ability Interface with other departments Inclination towards being process driven Punctuality and discipline Fluency in English Join us on our remarkable journey by applying right here.
Job date: Fri, 11 Feb 2022 23:25:42 GMT
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