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Clinical Research Associate II

ICON plc·Phoenix, Arizona

$91,336 - $114,170/yr·Full Time·Remote Ok·Remote friendly·2-5 yrs
·Posted 6 days ago
Practice for this role

About the role

Serve as the primary contact between investigational sites and sponsors while conducting various site visits including selection, initiation, and close-out. Ensure site compliance with ICH-GCP and regulations while managing data quality and patient safety reporting.

Clinical Research Associate - Oncology - West Region

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

What You Will Be Doing

  • Serve as the primary point of contact between investigational sites and the sponsor
  • Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out
  • Ensure site compliance with ICH-GCP, SOPs, and regulations
  • Maintain up-to-date documentation in CTMS and eTMF systems
  • Support and track site staff training and maintain compliance records
  • Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting
  • Support subject recruitment and retention efforts at the site level
  • Oversee drug accountability and ensure proper storage, return, or destruction
  • Resolve data queries and drive timely, high-quality data entry
  • Document site progress and escalate risks or issues to the clinical team
  • Assist in tracking site budgets and ensuring timely site payments (as applicable)
  • Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

You are

  • A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN
  • Eligible to work in United States without visa sponsorship
  • A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry
  • Experienced monitoring Oncology (i.e. Prostate Cancer, and Lung Cancer) and/or Hematology oncology.
  • Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
  • A clear communicator, problem-solver, and collaborative team player
  • Willing and able to travel up to 50% for on-site monitoring visits across the West region; preference given to candidates residing in Los Angeles, Phoenix, Seattle, Denver or Portland, near major HUB airports to support efficient regional travel

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits

may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits

may vary depending on role and location.

Visit our careers site [https://careers.iconplc.com/benefits] to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here [https://careers.iconplc.com/reasonable-accommodations].

Salary Range

$91,336.00-$114,170.00

Are you a current ICON Employee? Please click here [https://wd3.myworkday.com/icon/d/task/1422$1235.htmld] to apply

Requirements

Requires a Bachelor's degree in Life Sciences or RN qualification and at least 2 years of on-site monitoring experience in pharmaceutical or CRO industries. Must have specific experience in Oncology or Hematology oncology and be able to travel up to 50% within the West region.

  • bachelor degree
  • Regulatory Compliance
  • Subject Recruitment
  • eTMF
  • On-site Monitoring
  • CTMS
  • Site Management
  • Patient Safety Monitoring
  • ICH-GCP
  • Hematology Oncology
  • Drug Accountability
  • Oncology Monitoring
  • Clinical Trial Documentation

Posting details

Employment type
Full Time
Work arrangement
Remote Ok
Experience
2-5 yrs
Salary
$91,336 - $114,170/yr
Locations
Phoenix, Arizona; Denver, Colorado; Portland, Oregon; Seattle, Washington; Los Angeles, California; Blue Bell, South Dakota
Posted
Jul 23, 2026
Application
Employer website
IP

Hiring organization

ICON plc

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an...

Salary listed on 15 jobs
IndustryBiotechnology Research
TypePublic Company
Size10,001+ employees
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Market context

Arizona CRA II roles need oncology experience

In Arizona, Clinical Research Associate II roles are typically competitive because sponsors and CROs look for candidates with on-site monitoring experience, especially in Oncology or Hematology oncology, and the ability to travel up to 50% across the West region. This role category often draws steady demand from pharmaceutical and CRO teams, and this platform’s AI-summarized requirements and benefits help you review the original posting faster without extra research. Before applying, confirm your monitoring background matches the oncology focus and be ready to explain your regional travel availability.

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