# Senior CRA I

**Company**: Fortrea
**Location**: Beijing
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/FSP-SCRA-I--Beijing-_265305?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_da0e77f8-17d

## Description

The Senior CRA I is responsible for site monitoring and site management, ensuring clinical studies are conducted according to Standard Operating Procedures and Regulatory Guidelines.

**Responsibilities:**

- Conduct site monitoring, including routine monitoring and closeout of clinical sites, maintenance of study files, and pre-study and initiation visits.

- Manage site management as prescribed in project plans.

- Ensure study staff have proper materials and instructions to safely enter patients into the study.

- Verify informed consent procedures and protocol requirements are adhered to.

- Review source documents to ensure data integrity.

- Monitor data for missing or implausible entries.

- Perform monitoring tasks efficiently, managing travel expenses according to company policies.

- Prepare accurate and timely trip reports.

- Manage small projects under a Project Manager/Director.

- Serve as lead monitor for a protocol or project.

- Participate in protocol development and clinical trial report writing.

- Interact with internal work groups to evaluate needs, resources, and timelines.

- Coordinate clinical projects as a Local Project Coordinator.

**Qualifications:**

- University or college degree in life sciences or related field, or certification in a related allied health profession.

- Three years of clinical research experience in pharmaceutical or CRO industries.

- Thorough knowledge of regulatory requirements and drug development processes.

- Fluent in local office language and English.

**Experience:**

- Three years of clinical monitoring experience.

- Advanced site monitoring, study site management, and registry administration skills.

- Ability to work with minimal supervision and good planning and organisation skills.

- Valid driver's license.

**Physical Demands/Work Environment:**

- Travel requirements: 60-80% overnight.

## Skills

### Required
- clinical research
- site monitoring
- regulatory guidelines
- study management
- data integrity
- project management

### Nice to have
- local project coordination
- project management experience

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/FSP-SCRA-I--Beijing-_265305?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)