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From the employer's careers site First seen 28 Oct 2026

Clinical Research Associate - Early Development Multi Therapeutic - Regional (major hubs)

ICON Strategic Solutions Hybrid mid full-time

The employer hasn't listed a salary.

Apply on ICON Strategic Solutions

Description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

What you will be doing:

  • Serve as the primary point of contact between investigation sites and the sponsor for early development multi therapeutic clinical trials.
  • 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 early development Phase I/II clinical studies, across multiple therapeutic areas.
  • 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 60% for on-site monitoring visits; preference given to candidates residing 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.

Skills

Required

Ready to apply?

You apply with the employer directly. Their original posting is here: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Clinical-Research-Associate_JR155119

Apply on ICON Strategic Solutions