# Clinical Research Associate - Oncology

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

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Tennessee/Clinical-Research-Associate---Oncology_JR156932?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_1593072a-f07

## 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 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 (Prostate Cancer, and Lung Cancer) and/or Hematology Oncology clinical trials

- 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 Tennessee 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
- Oncology
- Hematology

### Nice to have
- Prostate Cancer
- Lung Cancer

---

Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Tennessee/Clinical-Research-Associate---Oncology_JR156932?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)