Arpita Borgaonkar Clinical Trial Operations, Clinical Research Assoc
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Theoretical knowledge does not totally help with practical circumstances
It is necessary to learn clinical research with real life experiences which I face in day to day life in organisation I work
I have passed Post Graduation recently thus I can help you with connecting bridge between academic knowledge and corporate real world knowledge
Keen Knowledge in NDCT, Codes of Ethics, USFDA m, EMA, MHRA Submissions is necessary which can be delivered with simpler form.
In addition Protocol designing, Informed Consent form designing and CRF preparation is my strength too.
Clinical research oriented Formula generation in MS Excel will help you in tracker making

Subjects

  • Good clinical practice (GCP) Beginner-Expert

  • BA/BE Clinical Trials Beginner-Expert

  • Phase I & II, RCT Phase II & RCT Phase III clinical trials Beginner-Expert

  • Clinical Research Associate Beginner-Expert

  • Codes Of Ethics-Clinical Trial Beginner-Expert

Experience

  • Clinical Research Associate (Feb, 2023–Present) at Centaur Pharmaceuticals Mumbai
    Foreseeing Trials
    Ethics submission dossier preparation
    Site TMF
    Trackers
    Case Report Form reviewing

Education

  • Ethics Review of Health Research (Feb, 2023–Feb, 2023) from Swayam Portal
  • Good Clinical Practices (Sep, 2022–Sep, 2022) from NIDA Clinical Trials Network
  • MSc. in Clinical Research (Sep, 2021–Jul, 2023) from SWAMI RAMA HIMALAYAN UNIVERSITY,JOLLY GRANT–scored 7.50

Fee details

    ₹500–1,000/hour (US$5.90–11.79/hour)

    More if travelling included

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