Chandru Kothandam

Experience

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  BioLim Centre for Science & Technology

  Dec 2019 - Dec 2019

  Research Intern

  Worked on Basis Study of Nanoparticles

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  Biocon Biologics

  Oct 2021 - Mar 2022

  Quality Assurance Quality Control

  Documented standard operating procedures (SOPs) according to ISO standards, Production Record Review. Involved in recording of all the data which all generated during manufacturing of the product (Batch Record Review). Trained on internal quality audits and quality review of product and out of specification investigations. Maintained records of release, separation or rejection of components and finished products, containers, closures and labels based on quality control test results. Inspected and tested products as per specification of RM, packaging, IP, FP, stability and shell life testing. Also involved in internal documentation Activity to organize, plan and implement QA/QC activities. Assisted with Manufacturing Qc team to Review and Assemble Documents.Exposure and Basic Training on Human Insulin Isophane(30-70), Insugen-R, Insulin Glargine, Insulin pen (Insugen M), MAbs, QMS, Packaging Quality Testing, Raw Material Analysis. Show less

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  Episource

  Jun 2022 - Jun 2022

  HCC Trainee

  Human Healthcare Coding and Chart Reviewing

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  Thryve Digital Health LLP

  Aug 2022 - Nov 2022

  Clinical Coordinator

  Reviewing Patient Medical Records and Clinical Data. Learnt about Medical coding and Healthcare Process. Had Training on HCPCS and ICD Codes Essential for timely Decision on processes. Had reviewed the entire Clinical Records of Patients at given time to take actions and Solutions to certain cases.Softwares Used : Predicle v2, InSinq, 4UM, Biscom, Power BI. Electronic Health Records (EHR)

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  Labcorp

  Dec 2022 - now

  Dose Scheduling - Events Reporting - Rees Review - QC - Material Ordering - Invoice - Shipments - Contracts Management - Client Management - HSE - Chemical Safety - Internal Auditing - CAPA - IATA - COSHHSoftwares/ Skills: Salesforce, Oracle DB, Data Visualization, Dashboard, Data Analysis, Macros, Microsoft Apps Working as Asst clinical Data analyst/ Data Associate I Day to day activities involve and includes Toxicology, GHS, CDM, SDS, ECHA, Database system, Pre clinical data, SAE, AE, Data analysis, Pathology and Histology, Regulatory Standards, CMC RA, QC Check, GxP, ICH-GCP, CAPA, Drug Development, Clinical Trials Data, Safety and Risk Assessment, Metabolism and CMC, Bio-Analytics.

  • Asst Clinical Data Analyst

    Jun 2024 - now

  • Clinical Data Associate I

    Dec 2022 - Jun 2024