# Senior CRA or CRA

**Company**: IQVIA
**Work arrangement**: hybrid
**Experience**: senior
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Ho-Chi-Minh-Vietnam/Senior-Clinical-Research-Associate-or-Clinical-Research-Associate_R1521946?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_44442127-561

## Description

This role offers you the opportunity to plan and progress your career as a Senior CRA or CRA at IQVIA, a leading global provider of clinical research services. You will have dedicated mentoring and receive structured quarterly reviews on performance, promotion opportunities and awards. Your responsibilities will include:

- Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation

- Supporting the development of a subject recruitment plan

- Establishing regular lines of communication plus administering protocol and related study training to assigned sites

- Evaluating the quality and integrity of site practices – escalating quality issues as appropriate

- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You will need to have a good knowledge of applicable clinical research regulatory requirements.

Qualifications:

- University degree in scientific discipline or healthcare

- At least 1 year of on-site monitoring experience

- Good knowledge of GCP and clinical research regulatory requirements

- Good computer skills including MS Office

- Excellent command of English language

- Organizational, time management and problem-solving skills

- Ability to establish and maintain effective working relationships with colleagues, managers, and customers.

- Flexibility to travel.

What you can expect:

- Working with different customers on global trials

- Career development opportunities for those who are passionate in wanting to grow as part of the organization.

- Leaders that support flexible work schedules/arrangement

- Excellent working environment in a stable, international, reputable company

- Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape

- Attractive remuneration package.

## Skills

### Required
- MS Office
- GCP
- clinical research regulatory requirements
- English

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Ho-Chi-Minh-Vietnam/Senior-Clinical-Research-Associate-or-Clinical-Research-Associate_R1521946?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)