Clinical Research Associate 2 – Oncology

Fortrea

. Provide a high standard of care for clinical trial participants and respond to emergency situations according to clinical research standards .

Posted 10/8/2026full-timeUnited StatesJuniorMid-Level💰 $100,000 - $112,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Monitoring and Oncology, ensuring compliance with clinical research standards and data integrity. Proficient in managing study sites, conducting monitoring visits, and training staff in a fast-paced environment.

Highest-signal resume keywords

Clinical Monitoring ExperienceOncology ExperienceNursing LicensureData Management SystemsStudy Site Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementData Integrity VerificationCRF ReviewSerious Adverse Event ReportingFeasibility Assessment

Soft Skills

TeamworkPeople SkillsAdaptability

Tools & Technologies

FortreaElectronic Data Environment

Certifications & Qualifications

University DegreeCertification in Allied Health Profession

Industry Keywords

Clinical Research StandardsInformed Consent ProceduresStudy Site MonitoringProject CoordinationVendor Liaison

About the role

Key responsibilities & impact

Provide a high standard of care for clinical trial participants and respond to emergency situations according to clinical research standards
Conduct all aspects of study site monitoring, including routine monitoring and close-out of clinical sites
Maintain study files and conduct pre-study and initiation visits
Liaise with vendors
Manage study sites according to project plans
Ensure study staff receive proper materials and instructions to safely enroll patients
Verify informed consent procedures and protocol requirements comply with applicable regulations
Ensure data integrity on Case Report Forms and other data collection tools
Monitor source data for missing or implausible data
Manage registries and undertake feasibility work when requested
Complete Serious Adverse Event reporting, reports, narratives, and follow-up
Perform CRF review, generate and resolve queries using Fortrea or client data management systems
Assist with training new employees through co-monitoring
Coordinate designated clinical projects as a Local Project Coordinator with supervision when applicable
Act as a local client contact when assigned
Perform other duties assigned by management

Requirements

What you’ll need

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
2 years of Clinical Monitoring experience
Oncology experience
Willingness and ability to travel 60% overnight
Ability to work in a fast-paced environment with changing priorities
Teamwork and people skills
Comfort working in a technology-based electronic data environment
Ability to sit for extended periods and operate a vehicle safely
Repetitive hand movement of both hands and ability to make fast, simple, repeated movements of the fingers, hands, and wrists
Occasional crouching and stooping, frequent bending and twisting of the upper body and neck
Ability to use varied computer software
Ability to lift and carry 15–20 lbs
Regular and consistent attendance
Availability to work varied hours

Benefits

Comp & perks

Remote work arrangement
60% overnight travel allowance/requirement
Ongoing applications accepted