ICON plc

Clinical Research Associate II

ICON plc$70K — $95K *
US-AnywhereRemote in West Palm Beach, FL
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences or equivalent, or qualified RN
  • 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry
  • Experience monitoring Oncology clinical studies (Prostate and Lung Cancer, Hematology Oncology)
  • Proficient in ICH-GCP and clinical systems like CTMS and eTMF
  • Clear communicator and collaborative team player
  • Eligible to work in the US without visa sponsorship
  • Willing to travel up to 50% within the southeast region, with preference for candidates residing in West Palm Beach, FL.

Responsibilities

  • Serve as the main contact between investigational sites and the sponsor
  • Conduct site visits including selection, initiation, monitoring, and close-out
  • Ensure compliance with ICH-GCP, SOPs, and regulations
  • Maintain documentation in CTMS and eTMF
  • Monitor patient safety and report adverse events
  • Support site staff training and maintain compliance records
  • Oversee drug accountability and ensure proper handling of investigational products
  • Document site progress and escalate issues to the clinical team.

Benefits

  • Competitive base salary and performance-related incentives
  • Health, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Learning and development opportunities through structured training.
Full Job Description
Clinical Research Associate - Oncology - West Palm Beach, FL

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 clinical studies
  • 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 southeast region; preference given to candidates residing in West Palm Beach, FL near major HUB airports to support efficient regional travel


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 to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

About ICON plc

ICON plc is a global provider of drug development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development. ICON has approximately 15700 employees in 40 countries. The company was founded in Dublin, Ireland in 1990 and is headquartered in Leopardstown, Dublin. ICON has been publicly traded on the NASDAQ since 1998.
Learn more about ICON plc
Size
39,300 employees
Market Cap
$16.2 billion
Industry
Net Income
$332.3 million
Founded
2017
5 Year Trend
+26.9%
Revenue
$2.7 billion
NASDAQ

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