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Clinical Research Associate - Oncology - Ohio / Western Pennsylvania

2-3 years
Not Disclosed
10 April 18, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Job Title:

Clinical Research Associate – Oncology (Ohio / Western Pennsylvania)


Location:

Pittsburgh, United States (Remote with Regional Travel in Ohio & Western Pennsylvania)


Job ID:

2025-118231


Department:

Clinical Monitoring – ICON Strategic Solutions


Job Type:

Full-Time, Remote


Application Contact:

Name: Monica Hawkins
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Job Description:

As a Clinical Research Associate (CRA), you will be working on multiple Oncology trials while being part of the world’s largest and most comprehensive clinical research organization. With a strong focus on quality of life and regional travel, this role allows you to build deep site relationships, coach junior monitors, and influence operational excellence.


Key Responsibilities:

  • Monitor and manage multiple Oncology clinical trials across regional sites

  • Act as a Lead Site Monitor (SM), mentor junior CRAs, and lead training efforts

  • Develop and review site start-up documents, SIV agendas, and monitoring guidelines

  • Represent Site Managers or Local Trial Managers on study management teams

  • Conduct quality reviews and support contract and budget negotiations

  • Participate in analysis and support visits (ASVs) and site qualification processes

  • Collaborate closely with cross-functional teams including Clinical Trial Assistants, LTMs, and Central Study Teams

  • Contribute to key KPIs and quality metrics per the Quality Oversight Plan (QOP)


Interfaces:

  • Primary: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager, Central Study Team

  • Other: Investigators, Study Coordinators, Site Pharmacists, Local Drug Safety Officers, Regional Compliance Teams


Required Qualifications:

  • Bachelor’s degree in Biological Sciences, Nursing, or related field (B.S., R.N., or equivalent)

  • Based in Western Pennsylvania or Ohio, near a major airport

  • 2–3 years’ experience in monitoring pharmaceutical industry clinical trials

  • 1–3 years’ experience monitoring Oncology trials

  • Experience with risk-based and analytical monitoring (preferred)

  • Knowledge of various clinical databases and systems (CTMS, EDC, eTMF, IWRS)

  • Strong GCP, ICH, and regulatory compliance understanding

  • Excellent communication, site management, and problem-solving skills

  • Ability to travel up to 50%

  • Must be legally authorized to work in the U.S. without future sponsorship


What ICON Offers:

  • Competitive salary with performance-based recognition

  • Health insurance packages tailored to you and your family

  • Retirement and savings planning support

  • Global Employee Assistance via TELUS Health

  • Paid annual leave and flexible work-life balance policies

  • Optional country-specific benefits: gym memberships, childcare vouchers, travel subsidies, etc.
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    Explore ICON Benefits


Diversity & Inclusion Commitment:

ICON values inclusion, belonging, and accessibility, ensuring equal opportunity for all qualified candidates without discrimination.