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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in patient safety, protocol compliance, and oncology clinical trial management, with a strong focus on interdisciplinary collaboration and regulatory adherence. Proficient in conducting patient screenings, managing research data, and providing education to clinical staff.
Highest-signal resume keywords
Oncology Clinical Trial ExperienceResearch Coordination ExperienceTexas or Virginia Registered Nursing LicensePatient Safety AdvocacyProtocol Compliance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Patient ScreeningData ManagementProtocol-Specific EducationAdverse Event ReportingEligibility DeterminationQuality Control ActivitiesSource Document MaintenancePharmacokinetic AssessmentsIntervention ImplementationElectronic Data Capture
Soft Skills
Interdisciplinary CommunicationCollaborationProblem-SolvingPatient EducationConfidentiality Management
Certifications & Qualifications
Registered Nursing License
Industry Keywords
Clinical ResearchOncology Care PracticesFederal RegulationsState RegulationsInstitutional PoliciesSOPsInformed ConsentStudy VisitsTeleconferencesQuality-of-Life Assessments
About the role
Key responsibilities & impact- Advocate for patient safety and protocol integrity
- Conduct patient screening and schedule and oversee on-study requirements
- Attend study teleconferences with sponsors and clinical research organizations
- Identify study objectives and outcome measures
- Adhere to federal, state, institutional, and NEXT Oncology research regulations, policies, procedures, and SOPs
- Communicate with interdisciplinary teams to ensure protocol compliance and timelines
- Collaborate with investigators, pharmacy, and personnel regarding study drugs
- Provide protocol-specific education to clinical staff
- Prepare for and conduct meetings and teleconferences with sponsors, monitors, and auditors
- Report serious adverse events, unanticipated problems, deviations, violations, and noncompliance
- Support informed consent and re-consenting processes
- Determine patient eligibility and educate patients and families about trial participation
- Coordinate protocol-required events, study visits, scans, pharmacokinetic/dynamic assessments, and quality-of-life collections
- Assess patient factors affecting adherence and implement interventions
- Evaluate adherence to protocol agents and treatment requirements
- Collaborate on disease response and treatment schedule or dose modifications
- Document patient encounters and maintain study and source documents
- Obtain outside provider and laboratory documents
- Ensure accurate source documentation and resolve discrepancies
- Maintain patient privacy and confidentiality
- Manage research data, troubleshoot data entry issues, and enter source data into CRFs and electronic data capture systems
- Participate in quality control activities and respond to database and sponsor queries
Requirements
What you’ll need- Knowledge of standard research and oncology care practices
- Typically requires 5 or more years of experience
- Current Texas or Virginia Registered Nursing License for RNs
- Bachelor's degree required for non-RNs
- Oncology clinical trial experience preferred
- Research Coordination experience preferred
Benefits
Comp & perks- Health and welfare benefits
- Incentive plans, bonuses, and/or other forms of compensation may be offered