Ashwini Chawade

Senior Clinical Research Coordinator at Spears Mind Research Solutions
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Contact Information
us****@****om
(386) 825-5501
Location
Ahmedabad, Gujarat, India, IN
Languages
  • English Hindi Marathi Gujarati -
Skills

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Credentials

  • Good clinical practice
    NIDA clinical trial networks
    Feb, 2022
    - Nov, 2024

Experience

  • Spears Mind Research Solutions
    • India
    • Research Services
    • 1 - 100 Employee
    • Senior Clinical Research Coordinator
      • Jun 2022 - Present

  • KV CLINICAL RESEARCH PVT LTD( Site Management Organization)
    • India
    • Research Services
    • 1 - 100 Employee
    • Clinical Research Coordinator
      • Feb 2022 - Jun 2022

  • Global Drug Development Experts, Nagpur
    • Acharya Vinoba Bhave Rural Hospital, Wardha (MH), India
    • Clinical Research Co-ordinator
      • Dec 2014 - Sep 2015

      • Schedule patient visits according to study protocol visit window. • Meet with patient research subjects and perform visit requirements. • Complete all Case Report Forms (CRFs) before all monitoring visits during the study. • Update study trackers for subject visits. • Performs Patient Visit Reminders, Visit Confirmations and/or Rescheduling of Visits i.e. due to investigator schedule change, subject requests a change and any other reason. • Confirm all required data is collected and transferred to case report. • Communicate with physicians, ancillary personnel, hospital department. • Communicate with Sponsor/ CRO to obtain required documents. • Coordinate with physicians, hospital, coordinators schedules and other departments for scheduling the trials and visits. • Maintaining study logs • Conduct site specific study feasibility. • Managing Clinical Research Department at site. Show less

  • Orange City Hospital & Research Institute
    • India
    • Hospitals and Health Care
    • 1 - 100 Employee
    • Clinical Research Co-ordinator
      • Aug 2013 - Jul 2014

      • Schedule patient visits according to study protocol visit window. • Meet with patient research subjects and perform visit requirements. • Complete all Case Report Forms (CRFs) before all monitoring visits during the study. • Update study trackers for subject visits. • Performs Patient Visit Reminders, Visit Confirmations and/or Rescheduling of Visits i.e. due to investigator schedule change, subject requests a change and any other reason. • Confirm all required data is collected and transferred to case report. • Communicate with physicians, ancillary personnel, hospital department. • Communicate with Sponsor/CRO to obtain required documents. • Coordinate with physicians, hospital, coordinators schedules and other departments for scheduling the trials and visits. Show less

Education

  • Acedamy For Ethical Clinical Research Training Institute, Nagpur
    P. G. DIPLOMA IN CLINICAL RESEARCH, Clinical Research
    2012 - 2013
  • Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur
    Master of Science - MS, Microbiology, General
    2009 - 2011
  • Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur
    M.Sc, ( Microbiology)
    2009 - 2011
  • Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur
    B. Sc Micrrobiology Chemistry Biotechnology
    2006 - 2009

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