Zydus Lifesciences Limited Released Job Openings On 29/10/2022.Zydus Cadila is one of the India’s leading healthcare companies and a global healthcare provider with a strength all along the pharmaceutical value chain. The groups state-of-the-art manufacturing infrastructure is spread across the five states Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim. Out of which, six facilities are USFDA approved. Zydus Lifesciences is headquartered in Ahmedabad, India, After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.
Vacancy Details:
Zydus Lifesciences Limited Recruiting B.Pharma,M.Pharma,M.Sc Graduates with 03-08 yrs of Experience for Deputy Manager Level-Pharmacovigilance(case processing) Position.Complete Details for the Deputy Manager Level-Pharmacovigilance(case processing) as follows.
Important Details :
- Job Location:Ahmedabad
- No of Vacancies:NA
- Details of Salary:NA
- Opening date for online Application: 29/10/2022
- 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
- Perform duplicate search in the global safety database and/or various logs/trackers using all possible/multiple criteria to identify the duplicate(s) of existing ICSR(s).
- Prioritize and process the cases retrieved/received from various sources like spontaneous, literature, regulatory, clinical studies/trials, BA/BE studies etc.
- Coding of events using the latest version of MedDRA and causality assessment of the reported events.
- Evaluation of the expectedness of the events by referring the latest PIs/SPCs/RSI/IBs.
- Writing the safety narrative.
- Perform follow-up with the reporter/author/concerned stake holder(s), as and when required.
- Coordinate with medical information contact center for collecting the follow-up information, as and when required.
- Quality review of the cases entered in the database for its quality and completeness.
- Submission of the eligible cases to regulatory agencies.
- Sharing of the eligible cases with concerned stake holder(s), as and when required.
- Attach/upload the acknowledgements of ICSRs in the global safety database.
- Resolve the queries related to the case processing activities.
- Update various logs/trackers related to case processing activities.
- Impart training on case processing activities to concerned stake holder(s), as and when required.
- Perform all other pharmacovigilance activities as assigned by HoD-GP
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