# Sr. CRA 2

**Company**: Fortrea
**Work arrangement**: remote
**Experience**: senior
**Job type**: full-time
**Salary**: $130 - $142K
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Remote-United-States/Sr-CRA-2--FSP-----Invitro-Diagnostics---West-Coast_265237-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_701d4355-79e

## Description

Our FSP team is currently seeking Sr. CRA 2s with 4+ years of monitoring residing in the Midwest US!

You will utilise your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

**Responsibilities**

- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned

- Responsible for all aspects of site management as prescribed in the project plans

- Conduct general on-site monitoring

- Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study

- Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements

- Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document monitoring and data verification

- Responsible for all aspects of registry management as prescribed in the project plans - undertake feasibility work when requested

- Complete Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow-up of SAEs

- Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management

- Assist with training of new employees, e.g. co-monitoring

- Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned

- Perform other duties as assigned by management

**Requirements**

- University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)

- 4+ years of Clinical Monitoring experience

- 50+% overnight travel

**Work Environment**

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

- Frequent travel to clients/site locations with occasional travel both domestic and international

**Physical Requirements**

- Ability to sit for extended periods and operate a vehicle safely

- Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists

- Occasional crouching, stooping, with frequent bending and twisting of upper body and neck

- Ability to access and use a variety of computer software developed both in-house and off-the-shelf

- Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs

- Regular and consistent attendance

- Varied hours may be required

**Target Pay Range:** $130 - $142K

## Skills

### Required
- Clinical Monitoring
- Clinical Trials
- Case Report Forms (CRFs)
- Serious Adverse Event (SAE) reporting
- Registry Management
- Site Management
- Data Review Guidelines

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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-2--FSP-----Invitro-Diagnostics---West-Coast_265237-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)