Melissa Ramgadoo, MHA, CCRC

Project Manager at Clinical Trial Media
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Contact Information
us****@****om
(386) 825-5501
Location
Queens County, New York, United States, US
Languages
  • English Full professional proficiency
  • Spanish Professional working proficiency
  • Hindi Limited working proficiency

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Credentials

  • Wrike Product Mastery: Silver Certificate
    Wrike
    Dec, 2022
    - Nov, 2024
  • Certified Clinical Research Coordinator
    Association of Clinical Research Professionals
    Sep, 2014
    - Nov, 2024
  • Certified Clinical Research Coordinator (CCRC®)
    Association of Clinical Research Professionals (ACRP)
    Sep, 2014
    - Nov, 2024
  • Phlebotomy
    Stony Brook Medicine
    May, 2013
    - Nov, 2024
  • Basic Life Support (BLS)
    American Heart Association | American Stroke Association
    Jun, 2010
    - Nov, 2024
  • National Health Institute Stroke Scale Certification
    National Institutes of Health
    Jun, 2010
    - Nov, 2024
  • Certified Clinical Research Coordinator (CCRC)
    ACRP - Association of Clinical Research Professionals

Experience

    • United States
    • Advertising Services
    • 100 - 200 Employee
    • Project Manager
      • Nov 2021 - Present

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Clinical Research Manager
      • Jul 2020 - Nov 2021

      -Oversees oncology clinical research activity pertaining to cancer clinical trials being conducted in the Cancer Clinical Trials Office (CCTO)-Provides leadership to team members and supervisors by communicating and guiding toward achieving department objectives-Develops and implements standard operating procedures within the CCTO-Collaborates with leadership to recommend, develop, implement, and oversee initiatives for the CCTO

    • Senior Certified Clinical Research Coordinator
      • Jul 2017 - Jul 2020

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Senior Clinical Research Coordinator
      • Dec 2016 - Jun 2017

      -Oversees the clinical assessments of the study subjects including but not limited to screening, evaluation and testing of the subjects. -Oversees data collection, processing, storage, inventory and quality control for clinical research studies. -Coordinates protocols and human subject approvals between various sites. -Analyzes highly complex data gathered on clinical research studies. -Interprets complex clinical research data. -Conducts clinical testing, develops protocols and assures all protocol procedures are approved. -Specializes in cancer clinical trials pertaining to breast oncology. Show less

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Clinical Research Coordinator
      • Jun 2010 - Aug 2015

      My experience includes assisting with the preparation of IRB submissions, maintaining appropriate correspondence with the IRB, sponsors, Principal Investigators (PIs), and Study Coordinators (SCs), creating Standard Operating Procedures (SOPs) for each study, negotiating sponsors' contracts/budgets, conducting subject visits, consenting, recruiting and retaining study patients, reporting adverse events, creating, preparing, and submitting case report forms (CRFs), conductions internal monitoring/auditing and study close-outs, and conducting clinical trials using good clinical practice (GCP). Show less

Education

  • Capella University
    Masters, Health/Health Care Administration/Management
    2018 - 2021
  • Stony Brook University
    Bachelor of Science (BS), Health Services/Allied Health/Health Sciences, General
    2008 - 2012

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