# Clinical Research Associate (CRA)

**Company**: Syneos Health
**Location**: BEL-Remote
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/BEL-Remote/CRA-Belgium---single-sponsor_25114309?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_f1b95149-65e

## Description

Syneos Health is seeking an experienced Clinical Research Associate (CRA) to join their team in Belgium. The successful candidate will be responsible for performing site qualification, site initiation, interim monitoring, site management activities, and close-out visits. They will also verify the process of obtaining informed consent, assess factors that might affect subject/patient's safety and clinical data integrity, and conduct source document reviews.

Responsibilities:

- Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits

- Verify the process of obtaining informed consent has been adequately performed and documented

- Assess factors that might affect subject/patient's safety and clinical data integrity

- Conduct source document reviews and verify required clinical data entered in the case report form (CRF) is accurate and complete

- Apply query resolution techniques remotely and on-site

- Utilize available hardware and software to support the effective conduct of the clinical study data review and capture

- Verify site compliance with electronic data capture requirements

- May perform investigational product (IP) inventory, reconciliation, and reviews storage and security

- Routinely review the Investigator Site File (ISF) for accuracy, timeliness, and completeness

- Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents

- Support subject/patient recruitment, retention, and awareness strategies

- Enter data into tracking systems as required

- Understand project scope, budgets, and timelines, and manage site-level activities/communication

- May act as primary liaison with study site personnel or in collaboration with Central Monitoring Associate

- Prepare for and attend Investigator Meetings and/or sponsor face-to-face meetings

- Provide guidance at the site and project level towards audit readiness standards

Qualifications:

- Bachelor's degree or RN in a related field or equivalent combination of education, training, and experience

- Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements

- Previous monitoring experience in Belgium

- Fluency in Dutch, French, and English

- Excellent communication, presentation, and interpersonal skills

- Ability to manage required travel for monitoring visits and work in the Wavre office on Mondays

## Skills

### Required
- Good Clinical Practice
- ICH Guidelines
- Dutch
- French
- English
- clinical research
- site management

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/BEL-Remote/CRA-Belgium---single-sponsor_25114309?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)