# Senior Clinical Research Associate - Oncology

**Company**: ICON Strategic Solutions
**Location**: Miami, FL
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Miami-FL/Senior-Clinical-Research-Associate_JR163352?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_945fffcc-94c

## Description

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

You will perform site management activities to support Oncology site success and maintain inspection readiness.

Key responsibilities include:

- Conducting site management activities to support client site success and maintain inspection readiness

- Acting as primary contact and facilitating communication between client's clinical trial team and sites

- Performing remote and on-site monitoring visits to ensure data integrity and subject safety

- Assessing monitoring quality and training less experienced CRAs

- Documenting monitoring activities and submitting visit reports

- Managing site essential document collection and TMF reconciliation

- Supporting sites with IRB/EC submissions and confirming approvals

- Reviewing site KRI metrics and resolving issues

- Developing and implementing site CAPA plans

- Delivering training to ensure site compliance with protocol, SOPs, GCPs, and regulations

- Supporting regulatory inspections and site identification

- Leading site engagement initiatives and fostering relationships with key Oncology sites

Requirements:

- Bachelor's degree in a scientific field

- 5+ years of monitoring clinical trials independently

- 2+ years of monitoring solid tumor clinical trials

- 1+ year of early development oncology trial experience and/or Phase III Oncology trial experience

- Solid tumor clinical trial experience

- Experience with Veeva systems is highly preferred

- Demonstrated experience in site relationships and securing compliance

- Expertise in GxPs and Oncology monitoring techniques

- Experience collaborating with sites and supporting regulatory inspections

- Willingness to travel up to 50%

ICON offers a competitive and comprehensive total rewards package, including:

- Competitive base salary and performance-related incentives

- Health and wellbeing programs

- Retirement and pension plans

- Life assurance and disability coverage

- Employee assistance programs and wellbeing resources

- Learning and development opportunities

## Skills

### Required
- GxPs
- Oncology monitoring techniques
- Risk-Based Monitoring
- Veeva systems
- Clinical trials monitoring

### Nice to have
- Early development oncology trial experience
- Phase III Oncology trial experience

---

Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Miami-FL/Senior-Clinical-Research-Associate_JR163352?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)