Summary
Overview
Work History
Education
Skills
Certification
Additional Information
Timeline
Generic

Carolina Granada

Senior Clinical Research Coordinator
Sugar Land,TX

Summary

Detail-oriented Research Coordinator familiar with documentation, reporting and compliance guidelines. Prepared to leverage expertise and 11 years of experience. Knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Ability to handle multiple projects simultaneously with a high degree of accuracy.

Overview

11
11
years of professional experience
8
8
years of post-secondary education
1
1
Certification

Work History

Senior Research Coordinator

Baylor College Of Medicine
08.2020 - 10.2022
  • Conducted hematology-oncology field research trials.
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Worked with principal investigator to facilitate daily trial activities and comply with research protocols.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Collected data and followed research protocols, operations manuals, and case report form requirements.
  • Followed informed consent processes and maintained records.
  • Maintained accurate and up-to-date case report forms and source documents for traceability.
  • Monitored patient safety throughout clinical trials and reported any adverse events.
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
  • Managed patient recruitment, informed consent process and data entry to support trial objectives.
  • Developed and maintained accurate and up-to-date case report forms and source documents.
  • Gathered, processed, and shipped lab specimens.

Senior Clinical Research Associate

Augusta University
08.2013 - 07.2020
  • Reviewed participant eligibility and consent documentation to help researchers achieve accurate and meaningful results.
  • Organized and maintained research study regulatory documents in site binder to maintain accuracy and integrity.
  • Followed drug storage procedures to comply with protocols and SOP requirements.
  • Collected data and followed research protocols, operations manuals, and case report form requirements.
  • Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Gathered, processed, and shipped lab specimens.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Followed informed consent processes and maintained records.
  • Prepared and maintained regulatory documents for clinical trial submissions.
  • Monitored patient safety throughout clinical trials and reported any adverse events.
  • Developed and maintained accurate and up-to-date case report forms and source documents.
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.

Research Assistant

Henry Ford Hospital
08.2011 - 08.2013
  • Organized research materials, maintaining a well-ordered workspace conducive to productivity.
  • Managed laboratory equipment and resources, ensuring proper maintenance and optimal functionality.
  • Maintained open lines of communication with project leads and team members for effective collaboration on common goals.
  • Streamlined data management processes for increased efficiency and accuracy in research findings.
  • Designed survey instruments tailored to specific research objectives for precise feedback gathering.
  • Created surveys and questionnaires to collect data for research projects.
  • Collaborate with senior research staff to support ongoing research projects related to Infectious Disease trials.
  • Assist in literature reviews and data collection efforts, contributing to the overall project goals.
  • Perform screening of research participants by applying strict inclusion and exclusion criteria to ensure the selection of suitable candidates for study participation.
  • Conduct data entry, cleaning, and organization tasks to ensure the accuracy and completeness of research datasets.
  • Participate in research team meetings, contributing ideas and insights to project discussions.
  • Attend relevant workshops, seminars, and training sessions to expand knowledge and skills in research methods and techniques.

Education

Master in Public Health - Epidemiology

University of Texas Health Science Center Houston
Houston, TX
08.2022 - 12.2024

M.D. -

Universidad Del Tolima
Ibague - Colombia
10.1996 - 10.2002

Skills

  • Data Collection

  • Ethics compliance

  • Participant screening

  • Study protocols

  • Specimen collections

  • Research experience

  • Informed consent

  • Specimen handling

  • Participant screening

  • Phlebotomy

  • Patient recruitment

  • Team Collaboration

Certification

Certified Clinical Research Coordinator (CCRC)

Additional Information

Publications


  • Patterns of venous thromboembolism risk, treatment, and outcomes among patients with cancer from uninsured and vulnerable populations.
    DOI: 10.1002/ajh.26623
  • Developing and optimizing a computable phenotype for incident venous thromboembolism in a longitudinal cohort of patients with cancer.
    DOI: 10.1002/rth2.12733
  • Effect of HIV/HAART and Other Clinical Variables on the Oral Mycobiome Using Multivariate Analyses. American Society for Microbiology. 03/23/2021

Timeline

Master in Public Health - Epidemiology

University of Texas Health Science Center Houston
08.2022 - 12.2024

Senior Research Coordinator

Baylor College Of Medicine
08.2020 - 10.2022

Certified Clinical Research Coordinator (CCRC)

10-2016

Senior Clinical Research Associate

Augusta University
08.2013 - 07.2020

Research Assistant

Henry Ford Hospital
08.2011 - 08.2013

M.D. -

Universidad Del Tolima
10.1996 - 10.2002

Similar Profiles

CREATE PROFILE
Carolina GranadaSenior Clinical Research Coordinator