Open To Work
Verified
This profile is verified using an email address.
Cierra DeNofa
Philadelphia,PA
Summary
ACRP-CP certified Clinical Research Professional with 2+ years of experience supporting oncology trials, patient engagement, and data integrity. Proven success managing multi-phase protocols (I–III) while ensuring regulatory compliance and workflow efficiency. Proficient in OnCore, Medidata RAVE, and EPIC; skilled in recruitment, screening, and data collection. Actively seeking new opportunities to expand clinical research expertise in dynamic, growth-driven settings. Actively looking to relocate to Florida, USA.
Overview
4
4
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator
Fox Chase Cancer Center
Philadelphia, PA
05.2024 - Current
- Coordinate and manage multiple oncology clinical trials, ensuring adherence to protocol requirements, FDA regulations, and ICH-GCP guidelines
- Conduct patient recruitment, screening, and enrollment, including eligibility verification and informed consent
- Oversee study visit scheduling, treatment timelines, and follow-up assessments to maintain protocol compliance
- Maintain regulatory binders, source documentation, and study records in audit-ready condition
- Support on-site and remote monitoring visits by preparing essential documents, resolving queries, and addressing findings
- Ensure accuracy between source documentation and EDC systems to support data integrity
- Collaborate with sponsors, CRAs, investigators, and interdisciplinary teams to ensure efficient trial execution
- Identify, document, and report adverse events in accordance with protocol and regulatory requirements
Clinical Research Data Specialist
Fox Chase Cancer Center
Philadelphia, Pennsylvania
11.2023 - 05.2024
- Managed data integrity and oversight for 17+ oncology clinical trials across multiple phases
- Performed data entry, query resolution, and data cleaning within multiple EDC systems
- Ensured alignment between EMR/source documentation and EDC data to mantain accuracy and compliance
- Supported monitoring visits by preparing source documents, regulatory materials, and study data reports
- Assisted in identifying and resolving data discrepancies and protocol deviations
- Contributed to site initiation, interim monitoring, and close-out activities
Research Assistant
Fox Chase Cancer Center
Philadelphia, Pennsylvania
05.2022 - 11.2023
- Facilitated patient recruitment for oncology clinical trials, enrolling over 800 participants.
- Maintained research databases and tracked key study metrics to monitor trial progress.
- Assisted in data collection, participant follow-up, and compliance with study protocols.
- Collaborated with research teams to ensure seamless daily operations of clinical trials.
- Supported researchers in preparing presentations and scientific reports for stakeholders.
Education
Bachelor of Science - Public Health
Temple University
Philadelphia, PA12-2020
Dual Enrollment Program - Psychology
Holy Family University
Philadelphia, PA01-2015
Skills
Clinical Trial Operations
- Protocol compliance
- Patient recruitment & enrollment
- Monitoring visit support
- Adverse event reporting (CTCAE familiarity)
Data & Systems
- Medidata Rave (EDC)
- Epic EMR
- OnCore CTMS
- Query resolution & data cleaning
Regulatory & Compliance
- ICH-GCP
- Regulatory binders & essential documents
- Audit readiness
- Source documentation
Certification
- ACRP-CP
Timeline
Clinical Research Coordinator
Fox Chase Cancer Center
05.2024 - Current
Clinical Research Data Specialist
Fox Chase Cancer Center
11.2023 - 05.2024
Research Assistant
Fox Chase Cancer Center
05.2022 - 11.2023
Bachelor of Science - Public Health
Temple University
Dual Enrollment Program - Psychology
Holy Family University