Dr.Manjunath Narayanagowda

Dr.Manjunath Narayanagowda

Duty Doctor

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location of Dr.Manjunath NarayanagowdaBengaluru, Karnataka, India

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  • Timeline

  • About me

    Proposal Development Manager @ MMS | Clinical Trials Expert

  • Education

    • Catalyst clinical services

      -
      Professional Diploma in Clinical Research (PDCR) Clinical Research
    • Cliniminds

      -
      Post Graduate Diploma in Pharmacovigilance Clinical/Medical Laboratory Science/Research and Allied Professions
    • Catalyst

      2011 - 2011
      PDCR Professional diploma in clinical research
    • Cliniminds

      2010 - 2010
      PGDPV PG diploma in Pharmacovigilance
    • Rajiv Gandhi University of Health Sciences

      -
      Bachelor of Ayurvedic medicine and Surgery (BAMS) Medicine
    • Rajiv Gandhi University of Health Sciences

      2000 - 2006
      BAMS Medicine

      Bachelor of Ayurveda Medicine and Surgery (BAMS)

  • Experience

    • Srinivasa nursing Home

      May 2005 - Mar 2007
      Duty Doctor

      Manage outpatient and inpatient.Minor OT procedures.

    • Quintiles cardiac safety services

      Mar 2007 - Dec 2010
      Cardilogy Associate

      -Evaluated the electrocardiographs (ECG) received as per ECG interpretation guidelines and project-specific requirements.-To be operationally responsible for their respective protocols as Operations Leader as an additional responsibility and Operation of different studies in collaboration with different study Coordinators.-To mentor, trainee Cardiology Associates and to help carry out their induction process. -Certified with distinction, by the Indian Society of Electrocardiology as competent ECG interpreter. عرض أقل

    • Quintiles cardiac safety services.

      Jan 2011 - Jul 2012
      Study specialist.

      Responsible for study deliverables to site within TAT with no compromise in quality reports along with resource management and training the team as per the study requirement.• Perform clinical quality control of the ECGs (paper/digital).• Assist in the induction process, mentoring and training of new Cardiology Associates.• Participate in planning for the study deliverables for the study assigned.• Identify risks involved in the study assigned and contribute to developing a risk management plan.• Monitor the study deliverables and produce regular updates for the same.• Assist in implementing lessons learned and continuous improvement exercises required as per ISO standards.• Ensure that the required documentation for the study is identified and completed.• Coordinate with the other teams involved in the study to ensure smooth conduct of the study. عرض أقل

    • MMS

      Jul 2012 - now

      • Coordinates with project management to develop, define, and negotiate project timelines• Coordinates with project team members to complete high quality deliverable by agreed upon timelines• Responsible for writing case narratives and producing high quality documents ensuring compliance with MMS quality processes throughout project lifecycle• Expert proficiency with styles of writing for various scientific document types and with client templates, toolbars, and style guides• Leads complex projects with multiple team members and independent coordination with the client• Overall management of the team عرض أقل Understand and adhere to narrative writing obligations by initiating and processing adverse event/serious adverse events/death/events of special interests narrative reports within approved timelines as defined in local and global work instructions, SOPs and regulations to meet local and global reporting requirements. Receive, prioritize and accurately transfer information from initial and follow-up source documents of adverse event/serious adverse events/death/events of special interests narrative reports to the appropriate fields. Assessment of case reports for seriousness, causality and expectedness.  Perform Case/Project initiation and processing duties as assigned. This includes but is not limited to receiving and tracking information regarding potential initial and follow up adverse event reports from all sources, prioritizing and providing reports to assigned staff members for assessment and assuring that cases are returned to narrative report validation/Quality check within defined timelines.  Collaborate in the review of written materials from peers including data collection, assessment, and other documents as provided by the client. عرض أقل

      • Proposal Development Manager

        Jan 2023 - now
      • Manager

        Jul 2022 - Feb 2023
      • Associate Manager

        Apr 2020 - Aug 2022
      • Senior Team Lead

        Oct 2017 - Mar 2020
      • Team Lead

        Sept 2014 - Sept 2017
      • Drug Safety Associate

        Jul 2012 - Aug 2014
  • Licenses & Certifications