Clinical Research Associate – Oncology

Trinity Health

. Coordinate and manage assigned oncology clinical trials from study start-up through closeout .

Posted 9/22/2026full-timeGrove City • Ohio • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing oncology clinical trials, including participant recruitment, data management, and regulatory compliance. Proficient in coordinating multidisciplinary teams and ensuring adherence to ethical research standards and GCP guidelines.

Highest-signal resume keywords

Oncology Clinical Trials ManagementElectronic Data Capture (EDC) SystemsRegulatory ComplianceParticipant RecruitmentClinical Research Data Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial MethodologiesData VerificationRegulatory Document PreparationAdverse Event ReportingProtocol Deviation Monitoring

Soft Skills

Effective CommunicationTime ManagementIndependent Work

Tools & Technologies

EDC Systems

Certifications & Qualifications

CITI Research Ethics Training

Industry Keywords

Oncology Research PracticesGCP StandardsHIPAA ComplianceParticipant SafetyEthical Research Conduct

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Coordinate and manage assigned oncology clinical trials from study start-up through closeout
Screen, recruit, and refer eligible research participants
Coordinate participant visits, assessments, treatments, laboratory testing, and follow-up activities
Serve as liaison among investigators, participants, sponsors, CROs, and internal clinical departments
Collect, review, verify, and enter clinical research data into EDC systems
Maintain regulatory binders, investigator site files, and essential study records
Prepare and submit regulatory documents, protocol amendments, continuing reviews, adverse event reports, and IRB correspondence
Monitor participant compliance and report protocol deviations
Track and resolve data queries, discrepancies, and missing information
Assist with adverse event and safety-related finding reports
Educate participants and clinical staff on study requirements and procedures
Protect participant confidentiality and health information under HIPAA
Collaborate with multidisciplinary healthcare teams to support protocol adherence and participant care
Support feasibility assessments, site activation, and enrollment initiatives
Prepare study updates, enrollment reports, and performance metrics
Participate in quality assurance activities, audits, inspections, and process improvement
Maintain knowledge of oncology research practices, regulatory requirements, GCP standards, and clinical trial methodologies
Promote participant safety, ethical research conduct, and patient advocacy
Perform other research-related duties as assigned

Requirements

What you’ll need

Bachelor's degree in biological sciences, health sciences, or medical field
CITI research ethics training required; on-site training provided
Two (2) to four (4) years of experience in clinical research required; oncology preferred
Experience using Electronic Data Capture (EDC) systems 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 access for eligible colleagues
Diversity, Equity, and Inclusion Colleague Resource Groups