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Clinical Research Associate - Oncology - Texas

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


Location:

Texas, United States (Remote – Regional Travel Required)


Job ID:

2025-118438


Department:

Clinical Monitoring – ICON Strategic Solutions


Job Type:

Full-Time, Remote (with up to 50% regional travel)


Application Contact:

Name: Monica Hawkins
Options: View other roles or send a message via the application platform


Job Description:

As a Clinical Research Associate (CRA) in Oncology, you’ll contribute to high-quality clinical trial execution with regional travel and a focus on quality of life. This remote role includes monitoring multiple oncology studies, acting as a lead or mentor for other Site Managers, participating in key operational activities, and supporting site start-up and study execution. This is an ideal opportunity for an experienced CRA looking to grow leadership skills and make an impact in cancer research.


Key Responsibilities:

  • Monitor multiple oncology trials with leadership responsibilities

  • Mentor junior staff and act as Lead Site Manager (SM)

  • Develop site start-up documents and lead training

  • Participate in SMT meetings, review study documents, and provide SM feedback

  • Support local trial budgets and site contract negotiations

  • Review reports (SQV, SMV, SCV) and assist with ASV

  • Collaborate with clinical teams, vendors, investigators, and site personnel

  • Ensure compliance with Good Clinical Practice (GCP), ICH, and local regulations

  • Track performance using defined KPIs as per Quality Oversight Plan


Required Qualifications:

  • Bachelor’s degree in Life Sciences, Nursing (R.N.), or equivalent

  • Based in Texas, near a major airport

  • 2–3 years’ monitoring experience in the pharmaceutical industry

  • 1–3 years’ experience in Oncology trials

  • Familiarity with multiple therapeutic areas is a plus

  • Experience with risk-based/analytical monitoring preferred

  • Skilled in CTMS, EDC, eTMF, IWRS, and safety reporting systems

  • Strong communication, relationship-building, and time management skills

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


Travel Requirement:

Up to 50% regional travel


What ICON Offers:

  • Competitive salary

  • Various annual leave entitlements

  • Diverse health insurance options

  • Retirement planning support

  • Global Employee Assistance Program (TELUS Health)

  • Life assurance

  • Flexible perks: gym discounts, travel subsidies, childcare vouchers, etc.
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    Explore ICON Benefits


Inclusion & Accessibility:

ICON is committed to fostering an inclusive, equitable, and accessible workplace.
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Request accommodations here