Faith C. Bashore
Clinical Research Coordinator (Phase 2/3 Clinical Trials)
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About
Highly self-motivated and organized clinical research professional with over a decade of experience in healthcare and research environments. Nearly two years of specialized experience in Phase 1 oncology clinical trials and extensive experience in Phase 2/3 neurology and cardiology studies. Skilled in protocol development, regulatory coordination, site management, safety monitoring, vendor oversight, and clinical data integrity.
Proficient in collaborating with Sponsors, CROs, PIs, and multi-disciplinary teams to execute studies with precision, compliance, and efficiency.
Experience
Clinical Research Coordinator (Phase 2/3 Clinical Trials) - Conquest Research - Arlington, VA
(2025-03)
- Develop study protocols specific to neurology/cardiology endpoints.
- Participate in feasibility assessments and site qualification.
- Draft and finalize study documents including protocols, IB, ICF, and CRFs.
- Coordinate neurological and cardiac assessments including EEG, ECG, MRI, and biomarkers.
- Support regulatory submissions including IND/CTA filings.
- Train site staff, manage vendors, and ensure operational readiness.
- Monitor patient safety, AE/SAE, and device malfunction reporting.
- Conduct monitoring visits and oversee data quality and protocol adherence.
- Manage IP accountability, imaging vendors, and external data sources.
- Support DSMB submissions, trend analysis, and safety signal tracking.
- Assist in database lock, CSR contribution, and inspection readiness.
Clinical Research Coordinator (Phase 1 Cancer Clinical Trials) - NEXT Oncology - Fairfax, VA
(2023-03 - 2024-08)
- Reduced protocol deviations by 20% through improved study alignment and execution.
- Partnered with interdisciplinary teams to ensure drug accountability and compliance.
- Delivered targeted drug handling training reducing medication errors by 15%.
- Improved SAE reporting efficiency by 20% through streamlined documentation processes.
- Enhanced patient consent accuracy by 15% through clarifying communication strategies.
Lead Clinical Research Associate - George Mason University - Fairfax, VA
(2020-01)
- Led operational teams with coaching, mentorship, and performance tracking.
- Managed timelines, budgets, and risk plans reducing operational delays.
- Oversaw CROs and vendor activities ensuring protocol compliance and quality.
- Supported protocol development and IRB submissions.
Lead Clinical Research Associate - Inova Fairfax Hospital - Fairfax, VA
(2022-07 - 2023-03)
- Developed study manuals reflecting regulatory and operational requirements.
- Led resource allocation, quality planning, and study milestone management.
- Coordinated national health system collaborations for NIH clinical trials.
Lead Clinical Research Associate - National Institutes of Health (NIH)
(2021-09 - 2022-07)
- Collaborated on protocol development and grant submissions.
- Managed IRB submissions including amendments and renewals.
- Coordinated implementation of national multi-site clinical trials.
Clinical Research Associate - Inova Translational Medicine Institute
(2016-07 - 2019-10)
- Maintained strong working relationships with interdisciplinary and external teams.
- Ensured regulatory compliance with GCP/ICH and FDA requirements.
- Managed monitoring activities within Medidata Rave EDC systems.
Clinical Research Assistant - Inova Translational Medicine Institute
(2012-07 - 2016-07)
- Screened patients according to protocol inclusion/exclusion criteria.
- Trained new research staff on screening and ethical conduct.
- Coordinated specimen collection and participant workflow.
Education
Bachelor of Science - Healthcare Administration - California Coast University
Associate Degree - ECPI College of Technology
