# Senior Clinical Research Associate (CRA)

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

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Buenos-Aires-Argentina/Senior-CRA_R1568729-2?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
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## Description

The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials. This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with regulatory requirements, and the overall success of clinical research projects.

Typical responsibilities 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

Requirements:

- A Bachelor's degree in a health care or other scientific discipline or educational equivalent

- At least 4 years of on-site monitoring experience

- Advanced in English

- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements

- Strong organizational and time management skills

- Excellent communication and interpersonal skills

- Ability to work independently and as part of a team

- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems

- Willingness to travel as required

## Skills

### Required
- GCP
- ICH guidelines
- regulatory requirements
- clinical trial management systems (CTMS)
- electronic data capture (EDC) systems
- English

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