Kiran Parab

Kiran Parab

M.sc in clinical research

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location of Kiran ParabThane, Maharashtra, India

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  • Timeline

  • Skills

    Inform
    Ich gcp
    Clinical data management
    Team management
    21 cfr part 11
    Microsoft office
    Microsoft excel
    Clinical research
    Protocol
    Edc
    Pharmaceutical industry
    Sas
  • About me

    Experienced Senior Clinical Data Coordinator with a demonstrated history of working in the hospital & health care industry. Skilled in Electronic Data Capture (EDC), Microsoft Excel, Clinical Research, Clinical Data Management, and SAS. Strong research professional with a Master focused in Clinical Research from Institute of Clinical Research.

  • Education

    • Institute of clinical research

      2009 - 2011
      Master clinical research

      1) completed my s.s.c in year 2004 from mumbai university.2) completed my h.s.c in year 2006(pcmb) from mumbai university. 3) completed my b.sc chemistry,drug and dies in year 2009 from mumbai university.4) m.sc clinical research in year 2011 for icri,mumbai

    • Institute of clinical research india

      2009 - 2011
      Pharmaceutical business management business administration, management and operations
  • Experience

    • Student at institue of clinical research india

      Aug 2009 - Aug 2011
      M.sc in clinical research
    • Tata consultancy services

      May 2011 - Sept 2014
      Senior process associate

      i have worked on discrepancy management, inform version 4.6 tool, sas checks. roles in current organization : review and understand the study protocol and the timelines. to be aware and updated of the glaxosmithkline quality standards and undertake any relevant training for the same if required.escalate any discrepancy in the clinical data to the dm study manager as appropriate.action study team feedback as required on the data.provide data listings in the required format as documented.perform external checks to handle and action the same manual discrepancies.review the resolved discrepancies and close where appropriate.providing query metrics as per request of query manager.coordinate with the glaxosmithkline cdm study manager with respect to any unresolved queries and close the same. to ensure an error free, quality data with no open queries.attend relevant study teleconference with the glaxosmithkline staff. show less

    • Cognizant

      Sept 2014 - Oct 2015
      Clinical data analyst
    • IQVIA

      Nov 2015 - Nov 2018
      Sr. clinical data coordinator
    • IQVIA Asia Pacific

      Nov 2018 - Sept 2020
      Associate data team lead

      working on all data team lead activities on start up and conduct phase.

    • Catawba Research

      Sept 2020 - Jun 2022
      Senior clinical data manager

      clinical data management - all start-up, conduct and close out activties.

    • Novartis

      Jun 2022 - now
      Principal clinical data manager
  • Licenses & Certifications

    • Balancing Work and Life

      LinkedIn
      Aug 2022