# Clinical Research Associate (CRA)

**Company**: IQVIA
**Work arrangement**: onsite
**Experience**: senior
**Job type**: full-time
**Salary**: $76,300.00 - $175,100.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/San-Juan-Puerto-Rico/CRA-2-Senior-CRA-1_R1559473?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_c8e155db-471

## Description

Join IQVIA, a leading global provider of clinical research services, and play a key role in delivering high-quality clinical trials as a Clinical Research Associate (CRA) based in Puerto Rico.

In this role, you'll partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and a strong focus on patient outcomes.

## Responsibilities

- Lead and execute site monitoring visits, including selection, initiation, routine monitoring, and close-out visits, in accordance with GCP/ICH guidelines.

- Build strong relationships with investigative sites to drive site performance, patient recruitment, and study engagement.

- Ensure protocol compliance, data integrity, and high-quality study execution.

- Proactively identify risks, resolve issues, and escalate concerns when appropriate.

- Track and manage study progress, including regulatory approvals, enrollment milestones, and data quality metrics.

- Maintain accurate study documentation and contribute to audit and inspection readiness.

- Collaborate with cross-functional teams to support successful study delivery and timeline achievement.

## What You Bring

- Bachelor's degree in Life Sciences, Healthcare, Nursing, or a related field (or equivalent experience).

- Minimum of 1.5 years of on-site monitoring experience as a Clinical Research Associate.

- Fluency in both English and Spanish (written and verbal) required.

- Experience monitoring studies in CNS, Cardiovascular, Obesity, and/or MASH/NASH therapeutic areas preferred.

- Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements.

- Excellent communication, relationship-building, problem-solving, and organizational skills.

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

- Ability and willingness to travel as required within Puerto Rico and potentially other locations as needed.

## Why Join Us

- Make a direct impact on advancing clinical research and improving patient outcomes.

- Work alongside experienced, collaborative, and mission-driven teams.

- Access opportunities for professional growth and career development.

- Thrive in a dynamic environment where your expertise and contributions truly matter.

The potential base pay range for this role, when annualized, is $76,300.00 - $175,100.00.

## Skills

### Required
- GCP
- ICH guidelines
- Life Sciences
- Healthcare
- Nursing
- English
- Spanish

### Nice to have
- CNS
- Cardiovascular
- Obesity
- MASH/NASH

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/San-Juan-Puerto-Rico/CRA-2-Senior-CRA-1_R1559473?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)