Inavolu Malavika

Experience

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  SYNCROP CLINCARE TECHNOLOGIES

  Apr 2017 - Feb 2018

  Internship Trainee

  .Learned basic core tablet preparation direct compression method.▪ Assisted in the evaluation of samples using weight variation, hardness, friability, In-Vitro disintegration time, andIn-Vivo dissolution studies.▪ Based on my background experience in work methods and monitoring, studied various departments and analyzed the organizational culture.

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  Dr. Reddy's Laboratories

  Apr 2017 - Jun 2017

  Industrial Trainee

  Insights of production, quality control, GMP, regulatory affairs.▪ Understanding the application of various instruments and pharmaceutical product analyses used in the industry,as well as the application of safety measures and techniques▪ Knowledge of the process functioning of the drugs, process parameters, particles, storage of drugs, and medicinal preparation by referring to SOP documents.

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  Università degli Studi del Piemonte Orientale

  Dec 2018 - Jul 2020

  Intern

  Provide the necessary research assistance in carrying out the included experiments and analyses.Extracting and storing genetic material from biological samplesAssisting with research article work

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  Università degli Studi di Torino

  Sept 2020 - Apr 2021

  Stem cells in Regenerative Medicine and Cell Factory Management

  Insights into standard cell culture and biochemistry techniques.Understanding how to use conventional, confocal, time-lapse, and dedicated analysis tools.Knowledge of Stem cell, regenerative medicine, and cell factory management

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  CCBR Clinical Research (Now Bioclinica)

  Mar 2021 - Nov 2021

  Junior drug safety associate

  Responsible for case intake, duplicate checking, and case registration.Review and evaluate AE case information to determine necessary action in accordance with internal policies and procedures and meet deadlines by processing all incoming cases.▪ Extensive coding of all medical history, events, drugs, procedures, indications, and laboratory tests using theappropriate dictionary (e.g., MedDRA, Company Product Dictionary, WHO-DD).▪ Writing medically relevant safety narratives about cases and checking the completeness and accuracy of the dataentered in the various fields and assist with ad hoc or routine safety monitoring activities.▪ Adhere to departmental workflow procedures, following up with sites regarding outstanding queries. Read on discrepancies' reconciliation. Perform any other drug safety-related activities and have the ability to mentor, handle given responsibilities with understanding. Show less

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  THE COUSNIL OF RESEARCH TRAINING SAS INSTITUTE

  Mar 2022 - Apr 2022

  BASE SAS

  Knowledge of working with SAS under platforms such as Windows 2000, XP.Knowledge of Base SAS, SAS Knowledge in the analysis of data for statistical analysis and reporting.Knowledge in producing external files and reports employing various SAS procedures, like Proc Import Export, Proc Append, Proc Print, Proc Freq, Proc Tabulate, Proc Means, and Proc Transpose.Knowledge of working with Excel, PowerPoint, and ODS HTML formatted files to produce Adhoc reports to the Users for Presentation and further Analysis. Export/extract data from databases and perform migration of data using Upload, Download. Show less

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  Selleck Chemicals LLC

  Sept 2022 - now

  Biology web editor