Research Nurse – Oncology

Trinity Health

. Coordinate education for stakeholders regarding new clinical trials and treatments .

Posted 9/17/2026full-timeGrove City • Ohio • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in coordinating clinical trials, managing patient care, and ensuring compliance with regulatory standards. Proficient in data management and effective communication with stakeholders in a clinical research environment.

Highest-signal resume keywords

Registered Nurse License in OhioOncology Clinical Nursing ExperienceClinical Research ExperienceResearch Regulatory KnowledgeEffective Communication Skills

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Patient Screening and EnrollmentCare ManagementData Collection and SubmissionRegulatory File MaintenanceInformed Consent AssistanceQuality AssuranceClinical Trial CoordinationProtocol Compliance

Soft Skills

Time ManagementIndependent Work Ability

Certifications & Qualifications

CITI Research Ethics Training

Industry Keywords

Clinical TrialsIRBInvestigational Drug ManagementPatient AdvocacyResearch Stakeholder Liaison

About the role

Key responsibilities & impact

Coordinate education for stakeholders regarding new clinical trials and treatments
Screen and enroll patients into appropriate clinical trials
Provide care management and coordination to ensure protocol compliance
Coordinate care among physicians, Mount Carmel, and study sponsors
Provide outpatient direct patient care and protocol-required inpatient assessments
Manage clinical trial data collection, submission, and query resolution
Prepare and maintain regulatory, IRB, and study files
Compile and submit information and data summaries
Serve as liaison and resource for internal and external research stakeholders
Advocate for patients participating in clinical trials
Plan and develop assigned research projects, including post-hospital follow-up plans
Assist physicians with informed consent
Coordinate investigational drug availability, storage, administration, and documentation
Assist with quality assurance and audit activities
Orient new research nurses and data collection and treatment staff
Provide cross-coverage for other research nurses
Attend IRB and committee meetings

Requirements

What you’ll need

Current license to practice as a Registered Nurse in Ohio
CITI research ethics training required (on-site training provided)
Minimum of five years of oncology clinical nursing experience
Demonstrated experience in the clinical research setting preferred
Effective communication skills
Knowledge of research regulatory and data management requirements
Ability to work independently
Strong time management skills

Benefits

Comp & perks

Competitive compensation and benefits packages including medical, dental, and vision with coverage starting on day one
Retirement savings account with employer match starting on day one
Generous paid time off programs
Employee recognition programs
Tuition/professional development reimbursement starting on day one
RN to BSN tuition 100% paid at Mount Carmel’s College of Nursing
Relocation assistance (geographic and position restrictions apply)
Employee Referral Rewards program
DailyPay for eligible colleagues
Diversity, Equity, and Inclusion Colleague Resource Groups