Dr. Bhanu Prasad

Dr. Bhanu Prasad

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location of Dr. Bhanu PrasadHyderabad, Telangana, India

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  • Timeline

  • About me

    Clinical Research Associate at Novartis

  • Education

    • Sri Indu Institute of Pharmacy

      2013 - 2019
      Doctor of Pharmacy

      • SRI INDU INSTITUTE OF PHARMACY (JNTUH), HYDERABAD, INDIA Pursued Doctor of Pharmacy (PHARM.D) with an aggregate of 82% - 2019. CORE SUBJECTS: Pharmacology, Clinical research, Medicinal chemistry, Pharmacotherapeutics, Biostatistics and Research methodology.

  • Experience

    • Aware Gleneagles Global Hospitals

      Jul 2017 - Jan 2018
      Observer

      Shadowed a variety of health professionals during their everyday routines.Assisted in collecting / confirming demographic information of patients in (E-Medra) EMR system for accurate patient tracking.Participated in ICU and ward rounds.Managed the follow up of patient cases from admission to discharge.Conducted inventory management to ensure proper tracking and ordering of needed supplies.

    • Clinwave Research Pvt Ltd

      Jan 2019 - Apr 2021
      Clinical Research Associate

      • Performing the Site Initiation, Monitoring and Close-out Visits. • Execute trials as per ICH-GCP guidelines and SOP of the Organization.• Reviewing the Trial procedures on sites to minimize the errors that profound during the trial.• Review trial procedures to minimize errors• Preparing the Clinical Trial Agreement between the CRO, Principal Investigator and Site (SMO)• Maintaining all the documents pertaining to the trial in Trial Master File.• Report any amendments to the Site Personnel for Ethics Committee with in the trial duration.• Manage and prepare source templates as per Study design in accordance with the CRF, provided by the sponsor. Show less

    • IQVIA India

      May 2021 - Aug 2022
      Associate Central Monitor

      1) Complete appropriate role-specific training to perform job duties.2) Perfroms assigned tasks to support team members with project execution (examples of such tasks include but not limited to running system reports, preparing and distributing status reports, creating and maintaining study documents, etc.)3) Interact with Sites / Clinical Research Asssociate and follow-up of missing data, pending queries, source data verification backlog, visit schedule, protocol deviations, etc.4) Assist in preparation of i-site pack for respective sites and countries for assigned studies.5) Perform the activities as per the task list delegated by Centralized Monitoring Specialist / Centralized Monitoring Lead.6) Assist in updating and maintaining data in systems within project timelines and per project requirement.7) Establish and maintain effective project / Site Communication.8) Create and maintain relevant project documents.9) Ensure accurate completion and maintenance of internal systems, databases, tracking tools and project plans.10) Act as a backup for Centralized Monitors. Show less

    • Novartis

      Aug 2022 - now
      Clinical Research Associate
  • Licenses & Certifications