Melissa Ramgadoo, MHA, CCRC
Project Manager at Clinical Trial Media- Claim this Profile
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English Full professional proficiency
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Spanish Professional working proficiency
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Hindi Limited working proficiency
Topline Score
Bio
Credentials
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Wrike Product Mastery: Silver Certificate
WrikeDec, 2022- Nov, 2024 -
Certified Clinical Research Coordinator
Association of Clinical Research ProfessionalsSep, 2014- Nov, 2024 -
Certified Clinical Research Coordinator (CCRC®)
Association of Clinical Research Professionals (ACRP)Sep, 2014- Nov, 2024 -
Phlebotomy
Stony Brook MedicineMay, 2013- Nov, 2024 -
Basic Life Support (BLS)
American Heart Association | American Stroke AssociationJun, 2010- Nov, 2024 -
National Health Institute Stroke Scale Certification
National Institutes of HealthJun, 2010- Nov, 2024 -
Certified Clinical Research Coordinator (CCRC)
ACRP - Association of Clinical Research Professionals
Experience
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Clinical Trial Media
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United States
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Advertising Services
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100 - 200 Employee
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Project Manager
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Nov 2021 - Present
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Northwell Health
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United States
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Hospitals and Health Care
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700 & Above Employee
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Clinical Research Manager
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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
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Senior Certified Clinical Research Coordinator
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Jul 2017 - Jul 2020
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Mount Sinai Health System
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United States
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Hospitals and Health Care
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700 & Above Employee
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Senior Clinical Research Coordinator
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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
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Stony Brook Medicine
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United States
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Hospitals and Health Care
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700 & Above Employee
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Clinical Research Coordinator
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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
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Education
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Capella University
Masters, Health/Health Care Administration/Management -
Stony Brook University
Bachelor of Science (BS), Health Services/Allied Health/Health Sciences, General