# Clinical Research Associate - Oncology

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

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Detroit-MI/Clinical-Research-Associate---Oncology---Detroit_JR143256?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
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## Description

As a Clinical Research Associate - Oncology at ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

You will serve as the primary point of contact between investigational sites and the sponsor - Oncology, conducting site visits, ensuring site compliance, and maintaining up-to-date documentation.

Responsibilities:

- Serve as primary point of contact between investigational sites and the sponsor - Oncology

- 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

- Collaborate with cross-functional partners

Requirements:

- Graduate with a Bachelor's degree in Life Sciences or equivalent, or a qualified RN

- Eligible to work in United States without visa sponsorship

- Clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry

- Experienced monitoring oncology clinical trials

- Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF

- Clear communicator, problem-solver, and collaborative team player

- Willing and able to travel up to 50% for on-site monitoring visits across Midwest region

Rewards & Benefits:

- Competitive base salary and performance-related incentives

- Health and wellbeing programmes, including medical, dental, and vision coverage

- 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

## Skills

### Required
- ICH-GCP
- CTMS
- eTMF
- Life Sciences
- Oncology

### Nice to have
- Oncology clinical trials
- Clinical research

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Detroit-MI/Clinical-Research-Associate---Oncology---Detroit_JR143256?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)