Marialby Donis Ramos

Clinical Research Coordinator at Sylvester Comprehensive Cancer Center
  • Claim this Profile
Contact Information
us****@****om
(386) 825-5501
Location
Miami-Fort Lauderdale Area

Topline Score

Topline score feature will be out soon.

Bio

Generated by
Topline AI

You need to have a working account to view this content.
You need to have a working account to view this content.

Experience

    • United States
    • Hospitals and Health Care
    • 300 - 400 Employee
    • Clinical Research Coordinator
      • Dec 2022 - Present

      • Assures that all protocol revisions, informed consents, continuing reviews, serious adverse events are submitted to the appropriate IRB of record in a timely manner. • Ensures study protocol adherence, including completion of protocol specific procedures and the completion of protocol specific documents while obtaining relevant medical information from patient clinic charts/medical records. • Establishes and maintains contact with patients/participants, health care providers, community agencies, study sponsors. Updates appropriate agencies such as sponsors, IRB, etc. regarding current status of research projects as required and under the supervision of the PI. • Maintains logs' progress reports to track both currently enrolled as well as follow-up participants. • Ensures data integrity and consistency in computer database and written records by reviewing entered data for accuracy. • Attends site disease group tumor board meetings and site disease group collaborative meetings. • Execute the plan developed for collection of protocol specific subject specimens, i.e. pharmacokinetics samples, blood specimen, tissue samples, etc. as per protocol. • Ensures that protocol lab kits and study specific supplies are obtained/ordered as necessary. • Ensures that randomization and registration of patients are performed in compliance with CRS and UM policies, the protocol, ICH-GCP, and federal regulations. • Communicates all IRB and Sponsor related approvals, changes, information, etc. to the PI and study team and adapts to physician schedules to perform protocol specific patient visits and/or procedures including, but not limited to early AM and /or early evening hours as required. • Participates in a collaborative, empowered work environment as demonstrated through teamwork and ensures work environment is organized and functions efficiently. Show less

  • Inpatient Research Clinic
    • Hialeah, Florida, United States
    • Clinical Research Coordinator
      • May 2022 - Dec 2022

      Planning and management of the studies, enrollment, maintenance, training initiatives, and maintaining compliance with federal, state, and institutional regulations. Planning and management of the studies, enrollment, maintenance, training initiatives, and maintaining compliance with federal, state, and institutional regulations.

    • Anesthesiology Resident
      • Sep 2018 - Jul 2021

    • Medical Intern
      • Aug 2017 - Jun 2018

      Achieve competence in interdisciplinary communication and participation. Record patient's medical history, vital statistics and information into charts, give preliminary diagnostics and participate in medical decisions. All of the above in the areas of Internal Medicine, Pediatrics, Obstetrics and Gynecology, Family medicine, and Surgery. Achieve competence in interdisciplinary communication and participation. Record patient's medical history, vital statistics and information into charts, give preliminary diagnostics and participate in medical decisions. All of the above in the areas of Internal Medicine, Pediatrics, Obstetrics and Gynecology, Family medicine, and Surgery.

Education

  • University of Medical Sciences of Ciego de Avila
    Doctor of Medicine - MD, Medicine
    2012 - 2018

Community

You need to have a working account to view this content. Click here to join now