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Clinical Research Coordinator

Location:
Denver, CO
Posted:
February 27, 2025

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Resume:

EVA ADANA

*** * ******* ***, ***** *** Englewood, CO 80113

**********.*****@*************.*** 720-***-****

PROFESSIONAL EXPERIENCE

Senior Clinical Research Coordinator

HCA (Swedish Medical Center) – Colorado

Feb 2025 – Present

- Lead and coordinate therapeutic studies in neurology and stroke, ensuring adherence to regulatory guidelines and study protocols.

-Oversee patient recruitment, enrollment, and monitoring, ensuring data integrity and participant safety throughout all study phases.

-Collaborate with investigators, neurologists, stroke specialists, and sponsors to maintain high standards of clinical research.

-Manage data collection, regulatory documentation, and CRF submissions, ensuring compliance with all applicable guidelines.

Clinical Research Coordinator II

HCA (Swedish Medical Center) – Colorado

Dec 2022 – Feb 2025

-Managed non-therapeutic oncology precision medicine trials, initiating and setting up research across two sites.

-Successfully recruited and enrolled participants, achieving top enroller status for multiple months at multiple sites.

-Built and maintained direct relationships with practices and physicians to enhance patient recruitment and trial engagement.

-Monitored patient safety, tracked adverse events, and ensured regulatory compliance.

-Managed data collection and submitted CRFs in a timely manner, ensuring quality and accuracy.

Clinical Research Coordinator

Children’s Hospital Colorado Anschutz Medical Campus – Colorado

Sept 2021 – Nov 2022

- Managed therapeutic pediatric trials, including cannabinoid-based studies for children with autism.

- Coordinated studies for sex chromosome disorders and Fragile X syndrome.

- Initially hired as a coordinator, but when the senior coordinator resigned, successfully managed the entire trial for 6 months, overseeing study operations and maintaining quality.

-Ensured protocol compliance, monitored patient progress, and maintained regulatory documentation.

-Collected data, reported adverse events, and collaborated with investigators to ensure study success.

Graduate Researcher

University of California, San Francisco (UCSF) – California

Aug 2020 – Aug 2021

-Conducted research on pediatric medulloblastoma mortality using electronic health record (EHR) data.

-Collaborated with oncologists, data scientists, and researchers to analyze and interpret clinical data.

-Presented findings at graduate conferences; manuscript currently in preparation for publication.

-Applied advanced statistical methods to ensure data integrity and accuracy.

-Research was recognized as one of the top 5 capstone projects in the Master's program.

EDUCATION

Master of Global Health Sciences

University of California, San Francisco (UCSF) Aug 2020 – Aug 2021

B.S. in Biology & B.A. in Musical Performance

Dominican University of California Aug 2016 – May 2020

Honors: Magna Cum Laude, Lillian L.Y. Wang Scholarship, Father Edwin Casey Endowed Scholarship

CERTIFICATIONS

Good Clinical Practice (GCP), Conflict of Interest, and FDA-Regulated Trials – CITI Program (Jan 2025)

Biomedical Researcher Certification – (Jan 2025)

PUBLICATIONS

CASCADE: CAnnabidiol Study in Children with Autism Spectrum Disorder

**The Effects of Thermal Stress on Montastraea cavernosa Aquacultured Corals

SKILLS

Clinical Trial Management: Protocol development, patient enrollment, monitoring

Data Analysis: Proficient in statistical software for clinical research

Regulatory Compliance: GCP, FDA, IRB, HIPAA compliance

EHR & Clinical Trial Software: Experienced with CTMS and EHR systems

Scientific Communication: Strong writing and presentation skills

Signature Date

Employee

Approver Date

Manager

Reference SOP: QMS-0900-WI-01 Page 1 of 1 ASSOC-DOC-049-SOP [D]



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