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Denise Flores

@deniseflores

Clinical Research Coordinator at Children’s Hospital Los Angeles, managing BMT trial operations, study data, and regulatory submissions.

United States

Message

What I'm looking for

I’m looking to contribute my knowledge and experience to support company goals and deliver quality work. I welcome new challenges and am comfortable working as part of a team or independently.

At Children’s Hospital Los Angeles, I managed daily operations and workflows for BMT trials. I maintained study data and regulatory files, and prepared specimens for analysis and shipment.

At KaiserPermanente, I evaluated, scheduled, recruited, enrolled, and consented patients for infectious disease research. I also managed study data and reviewed case report forms and informed consent documents for accuracy.

Earlier, I coordinated clinical research at So. California Institute for Respiratory Diseases and California Allergy and Asthma, supporting trial visits, regulatory compliance, and study procedures. I also worked as a Medical Assistant at Planned Parenthood, assisting with family planning and OB care.

Experience

Work history, roles, and key accomplishments

Clinical Research Coordinator I (BMT)

Children's Hospital Los Angeles

Sep 2024 - Jul 2026 (1 year 10 months)

Manage daily trial operations and workflows, maintain accurate source documents, case report forms, and regulatory files. Collect, record, and manage study data, screen and enroll eligible patients, and prepare specimens for analysis.

Clinical Trials Data Management Regulatory Compliance IRB Submission Specimen Handling Quality Assurance

Research Associate II

Kaiser Permanente

Feb 2022 - Apr 2024 (2 years 2 months)

Evaluated, scheduled, recruited, enrolled, and consented patients for clinical trials. Performed data management, collection, and entry, ensuring trials were conducted in accordance with FDA, ICH, and GCP guidelines.

Patient Recruitment Data Management GCP FDA Regulations ICH Guidelines Vital Signs Inventory Management

Medical Assistant

Planned Parenthood

Sep 2018 - Jan 2022 (3 years 4 months)

Obtained patient intake for family planning and OB care, educated clients, and handled referrals. Performed basic lab work, vital signs, and assisted clinicians with procedures.

Patient Intake Vital Signs Phlebotomy Lab Testing Medical Records Appointment Scheduling Insurance Verification

Clinical Research Coordinator

So. California Institute for Respiratory Diseases

Nov 2014 - Aug 2018 (3 years 9 months)

Ensured trials were conducted in accordance with FDA, ICH, and GCP guidelines. Facilitated study visits, reported adverse events, and performed study procedures including vitals, ECG, and spirometry.

Clinical Trials GCP FDA Regulations ICH Guidelines Adverse Event Reporting IWRS Drug Accountability ECG Spirometry Phlebotomy

Clinical Research Coordinator

California Allergy and Asthma

Mar 2007 - Nov 2014 (7 years 8 months)

Ensured trials were conducted in accordance with FDA, ICH, and GCP guidelines. Prepared exam rooms, scheduled patients, performed study procedures, and maintained regulatory documents.

Clinical Trials GCP FDA Regulations ICH Guidelines Regulatory Compliance Data Entry ECG Spirometry