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Oncology - Car-T - Cra Ii - Remote Us

Fortrea
Fortrea
1-3+ years
USD 105,000 – 117,000 per year
United States
10 Feb. 24, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Oncology – CAR-T Clinical Research Associate II (CRA II) – Remote USA

Location: Remote – United States (Major East & West Coast Hub Locations)
Category: Clinical Operations
Job ID: 26385
Employment Type: Full-Time
Travel Requirement: 60–70% (8–10 Days On Site per Month)
Experience Required: 1–3+ Years Clinical Monitoring Experience (Oncology Required; CAR-T Preferred)
Compensation: Target Pay Range USD 105,000 – 117,000 per year

About the Company

Fortrea is a global contract research organization delivering full-service clinical development solutions across oncology and other high-priority therapeutic areas. Through its Full-Service Outsourcing (FSO) model, Fortrea supports complex global trials with dedicated clinical operations expertise.

Role Overview

Fortrea is seeking experienced Oncology Clinical Research Associates (CRA II) with CAR-T exposure to support oncology trials across the United States. This role involves leading and monitoring advanced cellular therapy and oncology studies within a sponsor-dedicated environment.

The position is remote-based with substantial travel requirements to investigative sites nationwide.

Key Responsibilities

Clinical Site Monitoring & Management

  • Conduct pre-study, site initiation, routine monitoring, and close-out visits

  • Oversee all aspects of site management according to approved project plans

  • Maintain essential regulatory documentation in compliance with ICH-GCP and sponsor SOPs

  • Liaise with vendors and cross-functional stakeholders

Participant Safety & Regulatory Compliance

  • Ensure informed consent procedures meet regulatory requirements

  • Verify adherence to oncology protocol guidelines

  • Track, review, and follow up on Serious Adverse Event (SAE) reporting

  • Prepare and review SAE narratives and documentation

Data Quality & Source Verification

  • Perform source document verification (SDV)

  • Review Case Report Forms (CRFs) and electronic data capture systems

  • Identify missing or inconsistent data and generate queries

  • Independently manage query resolution within sponsor or CRO systems

Project Coordination & Leadership Support

  • Support registry management and feasibility assessments

  • Assist in training and co-monitoring junior CRAs

  • Serve as Local Project Coordinator when assigned

  • Act as sponsor contact at the site level under supervision

Educational Qualifications

  • University or college degree in Life Sciences preferred, OR

  • Certification in a related allied health profession (e.g., Nursing) from an accredited institution

  • Equivalent relevant experience may be considered

Experience & Competency Requirements

  • Minimum 1–3+ years of clinical monitoring experience

  • Mandatory experience in oncology clinical trials

  • CAR-T or cellular therapy trial experience strongly preferred

  • Strong understanding of Good Clinical Practice (GCP) and ICH Guidelines

  • Experience with SAE processing and regulatory reporting requirements

  • Strong communication, organization, and problem-solving skills

  • Ability to work independently in a matrixed, technology-driven environment

Work Environment

  • Remote/home-based role within the United States

  • 60–70% travel to clinical trial sites (8–10 DOS per month)

  • Occasional domestic and potential international travel

  • Office-based administrative work when not traveling

Physical Requirements

  • Ability to sit for extended periods and operate a vehicle safely

  • Frequent travel with light equipment (up to 15–20 lbs)

  • Repetitive computer-based documentation tasks

  • Flexibility to work varied hours based on study timelines

Compensation & Benefits

Eligible employees working 20+ hours per week may receive:

  • Medical, Dental, Vision, Life Insurance, STD/LTD

  • 401(k) Retirement Plan

  • Paid Time Off (PTO) – Flex Plan

  • Employee Recognition Programs

  • Employee Resource Groups (ERGs)

Why Consider This Opportunity?

This role provides direct involvement in innovative oncology and CAR-T clinical programs, supporting advanced cellular therapies that are transforming cancer treatment globally. It is ideal for experienced oncology CRAs seeking high-impact trials within a sponsor-dedicated FSO model.

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Explore more global oncology and clinical research career opportunities at ThePharmaDaily.com.