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Fsp - Sr. Cra 2 Or Cra 2 - Oncology - North East Us

Fortrea
Fortrea
2-4+ years
preferred by company
10 Jan. 6, 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

FSP – Senior CRA 2 / CRA 2 – Oncology (North East US)

Location: Multiple Locations, North East US
Job Type: Full-Time, Remote / Field-Based
Experience Required:

  • Senior CRA 2: 4+ years of clinical site monitoring experience, including oncology studies

  • CRA 2: 2+ years of clinical monitoring experience, including oncology studies
    Travel: Regional, ~30% overnight
    Job ID: 256121
    Category: Clinical Research / Oncology


About Fortrea

Fortrea is a leading global Clinical Research Organization (CRO) specializing in oncology and complex therapeutic trials. We partner with top pharmaceutical and biotechnology companies to advance clinical research, ensuring safe and compliant study execution while supporting patients and investigators.

This FSP-aligned role focuses on oncology clinical trials in the North East US, with opportunities to serve as a Local Project Coordinator or Lead CRA for assigned projects.


Role Overview

The Senior CRA 2 / CRA 2 – Oncology is responsible for monitoring clinical trial sites, managing site operations, and ensuring regulatory and protocol compliance. This role combines clinical expertise, project coordination, and team leadership to support oncology studies effectively.


Key Responsibilities

  • Conduct all aspects of study site monitoring, including initiation, routine visits, and close-out of clinical sites.

  • Ensure study staff receive proper protocol training and resources to safely enroll participants.

  • Maintain study files, regulatory documentation, and ensure audit readiness at site level.

  • Review Case Report Forms (CRFs) for accuracy, identify missing or implausible data, and resolve queries.

  • Oversee site management as outlined in project plans and SOPs.

  • Track, report, and follow up on Serious Adverse Events (SAEs), producing narratives and reports as required.

  • Support study feasibility, investigator recruitment, EC submissions, and regulatory communications.

  • Assist in protocol development, CRF design, and clinical trial reporting as assigned.

  • Act as lead monitor for assigned projects, including mentoring and training junior staff.

  • Manage study budgets, travel planning, and ensure efficient use of sponsor resources.

  • Coordinate study logistics, including vendor liaison, clinical supplies, and site resources.

  • Maintain compliance with Fortrea SOPs, GCP, and local regulatory requirements.


Required Qualifications

  • Education: University or college degree in Life Sciences preferred; nursing, medical, or allied health certifications accepted. Candidates with ≥3 years of relevant clinical research experience will also be considered.

  • Experience:

    • Senior CRA 2: 4+ years oncology clinical site monitoring

    • CRA 2: 2+ years oncology clinical site monitoring

    • SAE reporting, registry management, and advanced site monitoring skills required

  • Fluent in English, both written and verbal

  • Strong planning, organizational, and problem-solving skills

  • Ability to work independently and within a project team in a matrix environment

  • Valid driver’s license


Preferred Qualifications

  • Additional 1+ year of experience in clinical research, medical, pharmaceutical, laboratory, or technical writing roles

  • Local project coordination or project management experience

  • Prior experience with oncology study protocols and CRFs


Work Environment & Physical Requirements

  • Field-based with regional travel (~30% overnight); occasional domestic flights required

  • Work is performed in office and clinical environments with standard office equipment

  • Ability to sit for extended periods, operate a vehicle safely, and perform repetitive hand movements

  • Occasional bending, stooping, crouching, and lifting up to 20 lbs

  • Fast-paced, technology-driven environment where adherence to protocols is critical


Compensation & Benefits

  • Target Salary: $108,000 – $140,000 (based on title and experience)

  • Full-time or part-time employees (20+ hours/week) eligible for comprehensive benefits:

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

    • 401(K) retirement plan

    • Paid Time Off (PTO) and Flex Plans

    • Employee recognition programs

    • Access to multiple Employee Resource Groups (ERGs)


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