# Clinical Research Associate

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

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Budapest-Hungary/Clinical-Research-Associate--CRA-2-Sr-CRA-1----Sponsor-dedicated---Hungary_R1541627-2?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_39c46f2f-b67

## Description

We are seeking a Clinical Research Associate to perform monitoring and site management work. As a Clinical Research Associate, you will ensure that sites are conducting studies and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

**Responsibilities:**

- Perform site monitoring visits, including selection, initiation, monitoring, and close-out visits

- Work with sites to adapt, drive, and track subject recruitment plans in line with project needs

- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues

- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations

- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form completion and submission, and data query generation and resolution

- Ensure site documents are available for filing in the Trial Master File and verify that the Investigator's Site File is maintained in accordance with GCP/ICH and local regulatory requirements

- Create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans

- Collaborate and liaise with study team members for project execution support as appropriate

**Qualifications:**

- Bachelor's degree in a scientific discipline or healthcare preferred

- 1+ year of on-site monitoring experience

- Good therapeutic and protocol knowledge

- IT literacy

- Excellent written and verbal communication skills, including good command of English and Hungarian language

- Strong organizational and problem-solving skills

- Effective time and financial management skills

- Ability to establish and maintain effective working relationships with coworkers, managers, and clients

## Skills

### Required
- clinical research
- site management
- monitoring visits
- regulatory compliance
- English
- Hungarian

### Nice to have
- therapeutic knowledge
- protocol knowledge
- IT literacy
- organizational skills
- problem-solving skills

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Budapest-Hungary/Clinical-Research-Associate--CRA-2-Sr-CRA-1----Sponsor-dedicated---Hungary_R1541627-2?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)