# Clinical Research Associate II

**Company**: IQVIA
**Work arrangement**: onsite
**Experience**: senior
**Job type**: full-time
**Salary**: $74,500.00 - $197,500.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/Clinical-Research-Associate-2--IQVIA_R1570541?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_aa2fd346-b75

## Description

IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team.

We are looking for professionals with experience in one or more of the following therapeutic areas:

- Immunology/Gastroenterology (IM/GI)

- Dermatology

- Women's Health

- Asthma/Respiratory

- Ophthalmology

- HIV

**Job Overview** As a Clinical Research Associate II, you will conduct site selection, initiation, routine monitoring, and closeout visits in accordance with GCP, ICH, and applicable regulatory requirements.

Key responsibilities include:

- Building strong relationships with investigative sites and providing protocol, process, and study-specific training

- Monitoring study progress, including site activation, patient recruitment, enrollment, data collection, and query resolution

- Evaluating site performance and compliance, identifying risks and escalating quality concerns when appropriate

- Ensuring study documentation, regulatory records, and Trial Master File (TMF) requirements are maintained accurately and are inspection-ready

- Preparing monitoring reports, follow-up communications, and other required study documentation

- Collaborating with cross-functional study teams to support successful project delivery and achieve study milestones

- Supporting patient recruitment and retention initiatives at the site level

- Assisting with site financial and administrative activities, including invoice management, when applicable

**Qualifications**

- Bachelor's degree required

- Minimum 1 year of independent on-site monitoring experience in a CRO, biotech or pharmaceutical

- Working knowledge of GCP, ICH, and clinical trial regulations

- Strong communication, organizational, and problem-solving skills

- Proficiency with Microsoft Office applications

The potential base pay range for this role, when annualized, is $74,500.00 - $197,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

## Skills

### Required
- GCP
- ICH
- clinical trial regulations
- Microsoft Office applications
- communication
- organizational
- problem-solving

### Nice to have
- Immunology/Gastroenterology (IM/GI)
- Dermatology
- Women's Health
- Asthma/Respiratory
- Ophthalmology
- HIV

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/Clinical-Research-Associate-2--IQVIA_R1570541?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)