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

**Company**: ICON Strategic Solutions
**Work arrangement**: hybrid
**Experience**: mid
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Clinical-Research-Associate_JR155119?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_bebc5c42-584

## 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
- ICH-GCP
- CTMS
- eTMF
- Life Sciences
- clinical research

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Clinical-Research-Associate_JR155119?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)