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  • Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion Determine seriousness and relatedness across products as ...

  • Able to learn basics of SAS and start SAS Scripting. Extraction of Datasets from various databases to create SAS datasets. SAS Programming and Validation of Final Tables, Listings and Figures (TLFs) Programming and Validation of SAS domains

  • Follow up of indented material & receiving the indented material. Preparing receiving report on daily basis for the material received and paste quarantine labels. Maintaining Inward register and entry of Inward material in inventory control, COA numbering & filing. Good knowledge of SAP System. To coordinate with ADL for QC release and paste released label after approval. To coordinate for destruction of ...

  • Responsibilities, Skills & Experience required Pharma domain knowledge is Prefer Should have at least 3 years of experience in web development. Skills required on ASP, .net, MVC, Bootstrap angular & web api, jQuery on Oracle/ SQL database. Understand day to day requirement for development, modification and enhancement in existing software. Active Participation in designing architecture of enterprise software ...

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