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  1. Home
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  5. Sr. CRA II, Oncology, FSP
Fortrea logo

Sr. CRA II, Oncology, FSP

Not Disclosed•Full-TimeOn-site

location_on577, Mallard Avenue, Durham, Durham County, North Carolina, 27701, United States

Apply Now

About the Team

Our FSP team is dedicated to delivering high standards of care for participants in clinical trials. We operate in a fast-paced environment where precision is paramount; deviations from the study protocol are not tolerated, and meeting tight timelines is critical to maintaining quality.

About the Role

As an Oncology Sr. CRA 2, you will utilize your clinical judgment to manage all aspects of study site monitoring, from pre-study visits to close-out. Your mission is to ensure the protection of study patients by verifying adherence to informed consent procedures and regulatory requirements. You will safeguard data integrity by performing CRF reviews, generating queries, and resolving issues within our electronic data management systems.

This role requires you to adapt constantly to changing priorities while collaborating closely with site staff, vendors, and internal teams. You will also assist in training new employees and may act as a local client contact or Local Project Coordinator. Success in this position demands strong people skills and the ability to thrive in a technology-driven, dynamic setting.

Hiring Process

Applications are accepted on an ongoing basis. We look for candidates who are comfortable with the unique demands of our work environment, including frequent travel (40-50% overnight) and the ability to prioritize effectively under pressure.

Equal Opportunity

We are committed to creating an inclusive environment. Learn more about our EEO & Accommodations request here.

Work location

Work model: On-site

location_on

577, Mallard Avenue, Durham, Durham County, North Carolina, 27701, United States

Durham, North Carolina

Key Responsibilities

  • check_circleConduct routine and close-out monitoring visits for clinical study sites
  • check_circleManage study files and coordinate pre-study and initiation visits
  • check_circleAssist with training new employees through co-monitoring activities
  • check_circleCoordinate designated clinical projects as a Local Project Coordinator
  • check_circleReview source documents and Case Report Forms to ensure data integrity
  • check_circleVerify informed consent procedures and protocol adherence to protect patients
  • check_circleProcess Serious Adverse Event reporting, narratives, and follow-ups
  • check_circleGenerate and resolve data queries using clinical data management systems

Requirements

  • verifiedUniversity or college degree or certification in allied health profession
  • verified5+ years of Clinical Monitoring experience
  • verifiedOncology experience
  • verified40-50% overnight travel

Nice to Have

Oncology experience, early phase preferred

Fortrea cover image
Fortrea logo
Company

Fortrea

Industry

Biotechnology Research

Headquarters

Research Triangle Park, NC

Open Roles

1

Bringing life-changing benefits to patients faster

Fortrea, a clinical research organization based in Research Triangle Park, North Carolina, specializes in delivering clinical development solutions for the biotechnology and life sciences sectors. The company offers Phase I-IV clinical trial management, clinical pharmacology services, and consulting across more than 20 therapeutic areas. Fortrea supports biotech, biopharma, medical device, and diagnostic companies with full-service, functional-service, and hybrid models tailored to project needs. With operations spanning approximately 100 countries, Fortrea emphasizes scientific expertise and operational efficiency to meet the demands of clinical research. The organization leverages its legacy from predecessors Covance and Labcorp to provide scalable, innovative approaches for emerging and established clients. Fortrea’s focus on investigator site networks and regulatory compliance aims to streamline trial execution and advance medical innovation globally.

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Skills, education and keywords

Skills: Clinical Monitoring, Oncology, Nursing Licensure, Informed Consent Procedures, Protocol Requirements, Regulatory Requirements, Case Report Forms, Source Document, Serious Adverse Event Reporting, CRF Review.

Education: University or college degree in allied health or certification.

Frequently asked questions about Sr. CRA II, Oncology, FSP at Fortrea

What does a Sr. CRA II, Oncology, FSP at Fortrea do?expand_more
Day-to-day, the Sr. CRA II, Oncology, FSP at Fortrea will conduct routine and close-out monitoring visits for clinical study sites; manage study files and coordinate pre-study and initiation visits; assist with training new employees through co-monitoring activities; and coordinate designated clinical projects as a local project coordinator.
What are the requirements for this Sr. CRA II, Oncology, FSP role?expand_more
To qualify for the Sr. CRA II, Oncology, FSP at Fortrea position, applicants should have: University or college degree or certification in allied health profession; 5+ years of Clinical Monitoring experience; Oncology experience; and 40-50% overnight travel.
Where is the Sr. CRA II, Oncology, FSP role at Fortrea located?expand_more
Sr. CRA II, Oncology, FSP at Fortrea is based in 577, Mallard Avenue, Durham, Durham County, North Carolina, 27701, United States. This is a on-site role.
Is this Sr. CRA II, Oncology, FSP job remote, hybrid, or on-site?expand_more
Fortrea has listed this Sr. CRA II, Oncology, FSP role as on-site.
How much experience is required for this Sr. CRA II, Oncology, FSP role?expand_more
Sr. CRA II, Oncology, FSP at Fortrea typically requires 5+ years of relevant experience at the senior level.
What skills do you need for the Sr. CRA II, Oncology, FSP role at Fortrea?expand_more
Key skills for Sr. CRA II, Oncology, FSP at Fortrea include Clinical Monitoring; Oncology; Nursing Licensure; Informed Consent Procedures; Protocol Requirements; Regulatory Requirements; Case Report Forms; and Source Document.
What education is required for Sr. CRA II, Oncology, FSP at Fortrea?expand_more
Educational requirements for this role: University or college degree in allied health or certification.
What category does the Sr. CRA II, Oncology, FSP role belong to?expand_more
Sr. CRA II, Oncology, FSP at Fortrea is part of the healthcare & nursing job category on Recrutus.

About Fortrea

Fortrea, a clinical research organization based in Research Triangle Park, North Carolina, specializes in delivering clinical development solutions for the biotechnology and life sciences sectors. The company offers Phase I-IV clinical trial management, clinical pharmacology services, and consulting across more than 20 therapeutic areas. Fortrea supports biotech, biopharma, medical device, and diagnostic companies with full-service, functional-service, and hybrid models tailored to project needs.

With operations spanning approximately 100 countries, Fortrea emphasizes scientific expertise and operational efficiency to meet the demands of clinical research. The organization leverages its legacy from predecessors Covance and Labcorp to provide scalable, innovative approaches for emerging and established clients. Fortrea’s focus on investigator site networks and regulatory compliance aims to streamline trial execution and advance medical innovation globally.

Browse more roles: All Fortrea jobs, healthcare & nursing jobs on Recrutus.

Recrutus

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Search roles by city, category, skill, or job type — explore verified US employers, salary benchmarks, and remote-friendly teams hiring nationwide.

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View company profilearrow_forwardlanguageWebsitelinkLinkedIn
Quick Overview

Experience

5+ yrs (Senior)

Education

University or college degree in allied health or certification

Job Type

Full-Time

Skills Required

Clinical MonitoringOncologyNursing LicensureInformed Consent ProceduresProtocol RequirementsRegulatory RequirementsCase Report FormsSource DocumentSerious Adverse Event ReportingCRF Review
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