Oncology Clinical Research Associate II (CRA II) – Remote US
Locations: Open across 15 major US hubs – East & West Coast
Job Type: Full-Time, Remote
Experience Required: 1–3+ years in clinical monitoring; oncology experience preferred
About Fortrea
Fortrea is a leading clinical research organization delivering innovative clinical trial solutions. Our oncology team drives high-impact studies, including CAR-T and other cutting-edge therapies. Join a collaborative environment where clinical excellence, patient safety, and data integrity are prioritized.
Role Overview
We are seeking Oncology CRA II professionals to lead and support our Full-Service Outsourcing (FSO) team. This role involves clinical site management, monitoring, and regulatory compliance while maintaining the highest standards of patient safety and study quality. Candidates should be comfortable with frequent travel (60–70%, 8–10 days on-site per month) and working in a fast-paced, dynamic clinical environment.
Key Responsibilities
Conduct routine and close-out monitoring visits at clinical trial sites, including pre-study and initiation visits.
Ensure site staff are trained and equipped to follow protocol and safely enroll patients.
Verify patient safety and regulatory compliance, including informed consent procedures.
Maintain accurate study files and documentation.
Monitor data integrity through review of Case Report Forms (CRFs) or other data collection tools.
Conduct registry management and feasibility assessments as required.
Report and follow up on Serious Adverse Events (SAEs), including narratives and database updates.
Perform CRF review, query generation, and resolution using Fortrea or client data management systems.
Support training of new CRAs, including co-monitoring and mentoring.
Act as Local Project Coordinator for designated clinical projects and liaise with clients as needed.
Collaborate with cross-functional teams to meet study timelines and objectives.
Perform additional duties as assigned by management.
Qualifications & Requirements
University or college degree in nursing, life sciences, or allied health profession (licensed if applicable).
1–3+ years of clinical monitoring experience; oncology monitoring experience is highly desirable.
Comfortable working in a fast-paced, protocol-driven environment with constantly changing priorities.
Strong teamwork, communication, and interpersonal skills.
Proficiency with electronic data capture (EDC) systems and other clinical trial technologies.
Open to various hub locations across the US for remote work with travel.
Physical Requirements
Ability to sit for extended periods and operate a vehicle safely.
Repetitive hand movements and ability to handle laptops, documents, and study equipment (up to 15–20 lbs).
Occasional crouching, stooping, bending, and twisting.
Ability to maintain consistent attendance and work varied hours as required.
Benefits
Comprehensive medical, dental, vision, and life insurance.
Short-term and long-term disability coverage (STD/LTD).
401(k) retirement plan.
Paid time off (PTO) – flexible plan.
Employee recognition programs and ERG participation.
Competitive salary range: $105,000 – $117,000 annually (depending on experience and location).
Why Join Fortrea
Work on innovative oncology clinical trials, including CAR-T therapies.
Gain global exposure and professional growth opportunities.
Contribute to advancing cancer research while maintaining the highest clinical and ethical standards.
EEO & Accommodations
Fortrea is an equal opportunity employer. We are committed to providing an inclusive and accessible recruitment process. Accommodation requests will be confidential and considered to ensure equitable participation.
Apply Now
Join Fortrea’s oncology clinical research team and help deliver transformative therapies to patients worldwide.
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