# Senior Clinical Research Associate (Sr CRA 3)

**Company**: IQVIA Biotech
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Buenos-Aires-Argentina/Sr-CRA-3--Argentina--IQVIA-Biotech_R1559491-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
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## Description

IQVIA Biotech is seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to join the Clinical Monitoring team in Argentina.

The Sr CRA 3 will independently manage and monitor clinical trial sites to ensure studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, regulatory requirements, and sponsor expectations.

Key responsibilities include:

- Performing site monitoring activities such as site qualification, initiation, routine monitoring, and closeout visits

- Partnering with investigative sites to support patient recruitment and retention efforts

- Providing protocol and study-related training

- Proactively identifying and resolving quality or compliance issues

- Overseeing site performance, tracking study milestones, reviewing source documentation, managing data query resolution, and ensuring regulatory and essential documents are maintained

- Collaborating with cross-functional teams to support the successful execution of clinical trials

- Mentoring junior CRAs through co-monitoring and training activities

Requirements:

- Bachelor's degree in a scientific, healthcare, or related discipline (or equivalent combination of education and experience)

- Minimum of 4 years of on-site clinical monitoring experience

- Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical trial processes

- Experience conducting monitoring visits across multiple phases of clinical research

- Excellent organizational, communication, and problem-solving skills

- Ability to effectively manage multiple priorities in a fast-paced environment

- Proficiency with Microsoft Office applications and clinical trial systems

Preferred skills:

- Strong therapeutic area knowledge and protocol management experience

- Proven ability to build productive relationships with investigative sites, sponsors, and internal study teams

- Experience mentoring or supporting the development of junior clinical research professionals

## Skills

### Required
- Good Clinical Practice (GCP)
- International Council for Harmonization (ICH) guidelines
- FDA regulations
- clinical trial processes
- Microsoft Office applications
- clinical trial systems

### Nice to have
- therapeutic area knowledge
- protocol management
- mentoring

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Buenos-Aires-Argentina/Sr-CRA-3--Argentina--IQVIA-Biotech_R1559491-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)