# Clinical Research Associate

**Company**: IQVIA
**Work arrangement**: onsite
**Experience**: senior
**Job type**: full-time
**Salary**: $71,900.00 - $189,000.00
**Category**: Research
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Overland-Park-KS-United-States-of-America/Sr-CRA--Sponsor-Aligned--Oncology_R1541483?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_933ad722-fad

## Description

Join IQVIA as a Clinical Research Associate, playing a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements.

Key Responsibilities:

- Conduct site monitoring visits in line with GCP and ICH guidelines, including selection, initiation, monitoring, and close-out visits.

- Collaborate with sites to develop and track recruitment plans, ensuring project needs are met.

- Provide protocol and study training to sites, maintaining regular communication to manage expectations and address issues.

- Assess site practices for protocol adherence and regulatory compliance, escalating quality issues as needed.

- Oversee regulatory submissions, recruitment, enrollment, CRF completion, and data query resolution.

- Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF) per GCP/ICH and local regulations.

- Generate visit reports, follow-up letters, and other necessary documentation.

- Mentor clinical staff through co-monitoring and training visits.

- Work closely with study team members to support project execution.

Qualifications:

- BS degree required; a degree in a scientific discipline or healthcare is preferred.

- 3+ years of on-site oncology monitoring experience strongly preferred; 1.5+ years of oncology monitoring experience can be considered.

- Phase 1 oncology experience is required.

Skills:

- Proficient in GCP and ICH guidelines.

- Strong therapeutic and protocol knowledge in Phase 1 oncology trials.

- Excellent computer skills, including Microsoft Office and mobile devices.

- Effective communication, organizational, and problem-solving abilities.

- Strong time management skills.

- Ability to build and maintain effective working relationships.

Why Join Us? Be part of a team that's pushing the boundaries of cancer research, working on cutting-edge Phase 1 oncology trials, collaborating with top professionals, and contributing to life-changing advancements in cancer treatment.

The potential base pay range for this role, when annualized, is $71,900.00 - $189,000.00.

## Skills

### Required
- GCP
- ICH guidelines
- Phase 1 oncology trials
- Microsoft Office

### Nice to have
- oncology monitoring experience

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Overland-Park-KS-United-States-of-America/Sr-CRA--Sponsor-Aligned--Oncology_R1541483?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)