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Quality Control Coordinator
Georgetown University Center on Education and the Workforce. Perform quality control assessments and risk-based centralized eligibility reviews for select cancer clinical trials, such as NCTN studies .
Posted 11/11/2026full-timeWashington, D.C. • District of Columbia • United StatesJuniorMid-Level💰 $44,022 - $73,407 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in quality control assessments, compliance with regulatory standards, and clinical trial management, particularly within oncology research. Proficient in data integrity verification and audit preparation, with strong organizational and communication skills.
Highest-signal resume keywords
Clinical Research ExperienceGood Clinical Practice (GCP)Quality Control ReviewsAudit Preparation ProcessesSOCRA/CCRP Certification
ATS Keywords
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Hard Skills
Quality Control AssessmentsSource Document VerificationCentralized Eligibility ScreeningClinical Trial WorkflowsProtocol Discrepancy Identification
Soft Skills
Organizational SkillsProblem-Solving SkillsVerbal Communication SkillsWritten Communication SkillsPresentation Skills
Tools & Technologies
Clinical Trials Management System (CTMS)OnCoreMicrosoft OfficeGoogle Workspace
Certifications & Qualifications
SOCRA CertificationCCRP CertificationACRP CertificationCCRC CertificationCCRA Certification
Industry Keywords
FDA GuidelinesHuman Subject ProtectionICH GuidelinesNCI Cancer Center Support Grant (CCSG)Oncology Therapeutic Research
About the role
Key responsibilities & impact- Perform quality control assessments and risk-based centralized eligibility reviews for select cancer clinical trials, such as NCTN studies
- Conduct regular quality reviews in the Clinical Trials Management System (CTMS; OnCore) to assure data integrity and SOP compliance
- Assist with coordination, preparation, conduct, and follow-up for internal quality monitoring and external audits across LCCC consortium sites
- Collaborate with ORQA and the TEQC Manager to review audit findings and identify systemic trends for future training and education
- Assist with maintaining Lombardi CTO Standard Operating Procedures and Guidance Documents
- Verify adherence to Lombardi CTO Guidance Documents, GUMC and MedStar Health SOPs, and applicable regulatory standards
- Support staff competency and promote audit readiness across LCCC cancer clinical research studies
- Work in compliance with Human Subject Protection, HIPAA, and GCP guidelines
- Interact with clinical research faculty, staff, consortium teams, institutional departments, sponsors, external monitors, and regulatory inspectors
Requirements
What you’ll need- Bachelor’s degree in a biological science, health science, or related field
- Ability to perform light travel to consortium sites, as needed
- Working knowledge of FDA, Human Subject Protection, Good Clinical Practice (GCP), and ICH guidelines
- Foundational understanding of medical and clinical research terminology, protocol visit structures, and clinical trial workflows, preferably within oncology therapeutic research
- Understanding of quality control reviews, source document verification, centralized eligibility screening, and audit preparation processes
- Proven ability to review clinical research records accurately, identify protocol discrepancies or compliance gaps, and document findings clearly
- Strong organizational and problem-solving skills, with the ability to prioritize competing tasks and deliver high-quality results within defined timelines
- Strong verbal, written, and presentation skills
- Proficiency with Microsoft Office (Word, Excel, PowerPoint), Google Workspace, and CTMS (OnCore)
- Up to two (2) years of clinical research experience, preferably in oncology clinical trials
- Knowledge of or prior experience with NCI Cancer Center Support Grant (CCSG) guidelines and expectations
- SOCRA/CCRP or ACRP/CCRC/CCRA certification
Benefits
Comp & perks- Medical, dental, vision, disability, and life insurance
- Retirement savings
- Tuition assistance
- Work-life balance benefits
- Employee discounts
- Voluntary insurance options
- Professional development opportunities
- Community involvement opportunities