# Senior CRA II

**Company**: Fortrea
**Experience**: senior
**Job type**: full-time
**Salary**: $130-133K
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Remote-United-States/Sr-CRA--FSP---Surgical---Medical-Device---Central-region_266196?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_c5d4b311-c51

## Description

Fortrea's FSP team is seeking experienced Central based Sr. CRAs with 1+ year of device experience. The role involves site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines.

The Senior CRA II is responsible for:

- Site monitoring and site management

- Implementing project plans

- Leading projects of limited scope

- Acting as Local Project Coordinator or Lead CRA

- Ensuring study staff have proper materials and instructions

- Protecting study patients by verifying informed consent procedures and protocol requirements

- Ensuring data integrity through source document review

- Monitoring data for missing or implausible entries

- Managing travel expenses efficiently

- Preparing accurate and timely trip reports

- Managing small projects under a Project Manager/Director

- Serving as lead monitor for a protocol or project

- Reviewing project progress and initiating actions to achieve targets

- Organizing presentations at Investigator Meetings

- Participating in protocol and Case Report Form development

- Interacting with internal work groups

- Acting as contact for clinical trial supplies and vendors

- Managing registry aspects as prescribed in project plans

- Conducting feasibility work and Quality Control visits

- Recruiting investigators and preparing EC submissions

- Negotiating study budgets and assisting with agreements

- Tracking Serious Adverse Event reporting

- Performing CRF reviews and query resolution

- Assisting with training and development of new employees

**Qualifications:**

- University or college degree in life sciences or related field

- Certification in a related allied health profession

- 3+ years of Clinical Monitoring experience

- Thorough knowledge of regulatory requirements

- Understanding of the drug development process

- Fluent in local office language and English

**Experience:**

- Advanced site monitoring skills

- Advanced study site management skills

- Ability to work with minimal supervision

- Good planning and organization skills

- Good computer skills

- Advanced verbal and written communication skills

- Ability to train and supervise junior staff

- Valid Driver's License

**Physical Demands/Work Environment:**

- Travel requirements: 60-80% overnight

- Work is performed in an office environment with exposure to electrical office equipment

- Occasional drives to site locations with occasional travel both domestic and international

**Target Pay Range:** $130-133K

## Skills

### Required
- Clinical Monitoring
- Site Management
- Regulatory Compliance
- Data Integrity
- Project Management
- Communication
- Leadership

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Remote-United-States/Sr-CRA--FSP---Surgical---Medical-Device---Central-region_266196?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)