# Experimented CRA France - single sponsor

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

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/FRA-Remote/Experimented-CRA-France---single-sponsor_25107483?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_b95b9b6d-9c8

## Description

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. The role of Experimented CRA France - single sponsor involves conducting on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.

**Job Responsibilities**

- Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms

- Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates

- Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials

- Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues

- Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans

- Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct

**Qualifications:**

- Bachelor's degree in a related field or equivalent experience

- Minimum of 2-4 years of experience in clinical research monitoring

- Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements

- Excellent communication and interpersonal skills

- Ability to work independently and manage multiple priorities

- Proficiency in using clinical trial management systems and other relevant software

**Certifications:**

- Certified Clinical Research Associate (CCRA) or equivalent certification preferred

**Necessary Skills:**

- Attention to detail and strong analytical skills

- Problem-solving abilities and critical thinking

- Ability to work effectively in a team environment

- Strong organizational and time management skills

- Proficiency in Microsoft Office Suite

## Skills

### Required
- Good Clinical Practice (GCP)
- clinical research monitoring
- clinical trial management systems
- Microsoft Office Suite

### Nice to have
- Certified Clinical Research Associate (CCRA)

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/FRA-Remote/Experimented-CRA-France---single-sponsor_25107483?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)