Overview
Work History
Timeline
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MIA E. SHARPE

Orlando,USA

Overview

10
10
years of professional experience

Work History

Clinical Research Coordinator

CareAccess
Orlando, FL
01.2023 - Current
  • Assisting in screening patients, obtaining Informed Consent from the patient, maintaining patient charts organized
  • Formulate observations, note results in CRF/eCRF/Source documentation systems
  • Draw inferences about trial assessments and report on conclusions
  • Prepare lab specimens for delivery to reference laboratory
  • Ensure proper handling of specimens according to in-house/reference laboratory protocols
  • Ensure lab specimens are appropriately labeled with proper test(s) ordered, correct accession number, tube type, etc. required to perform necessary procedures
  • Provide research support by preparing trial assessments, analyzing data, perform comparative analyses from former experimental data
  • Notify lab processor of any issues with orders and/or lab specimens
  • Develop research papers for publication based on experimental results and analysis

Clinical Research Coordinator

APG Research, LLC
Orlando, FL
02.2022 - 11.2022
  • Assisting in screening patients, obtaining Informed Consent from the patient, maintaining patient charts organized
  • Formulate observations, note results in CRF/eCRF/Source documentation systems
  • Draw inferences about trial assessments and report on conclusions
  • Prepare lab specimens for delivery to reference laboratory
  • Ensure proper handling of specimens according to in-house/reference laboratory protocols
  • Ensure lab specimens are appropriately labeled with proper test(s) ordered, correct accession number, tube type, etc. required to perform necessary procedures
  • Provide research support by preparing trial assessments, analyzing data, perform comparative analyses from former experimental data
  • Notify lab processor of any issues with orders and/or lab specimens
  • Develop research papers for publication based on experimental results and analysis

Clinical Research Coordinator

SIH Research – Mumtaz
Kissimmee, FL
06.2019 - 01.2022
  • Obtained Informed Consent Forms, enrolled subjects into clinical trials where eligible
  • Scheduled/obtained patient information including medical history, EKG information and any biological samples as specified in each respective protocol
  • Formulated, prepared, and maintained source documentation while preparing patients for specific trial assessments as specified per the protocol
  • Assist Principal Investigator with patient examination and administration of investigational product
  • Collected and processed patient specimens for select diagnostic tests
  • Serves as liaison between physician and other business affiliates
  • Managed practice finances and inventory of office materials/equipment

Clinical Research Coordinator

Rheumatology Associates
Orlando, FL
09.2015 - 05.2019
  • Received/logged each specimen received in EDC system with proper identification, collection dates and sample types
  • Formulated observations and made note of results of experiments
  • Reported on conclusion of experiments conducted
  • Prepared biological specimens for pick-up to reference lab and ensured proper handling according to in-house or reference laboratory protocols
  • Ensured all specimens sent out to reference labs were appropriately labeled with proper test(s) ordered, correct accession number, tube type, and number of types required to perform the required tests
  • Provided research support by preparing experiments, analyzing data, and performing comparative data analyses from previous experimental data

Timeline

Clinical Research Coordinator

CareAccess
01.2023 - Current

Clinical Research Coordinator

APG Research, LLC
02.2022 - 11.2022

Clinical Research Coordinator

SIH Research – Mumtaz
06.2019 - 01.2022

Clinical Research Coordinator

Rheumatology Associates
09.2015 - 05.2019

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MIA E. SHARPE