# Clinical Research Coordinator

**Company**: IQVIA
**Location**: Fairfax, VA
**Experience**: mid
**Job type**: full-time
**Salary**: $43,400.00 - $108,200.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Fairfax-VA-United-States-of-America/Day-LPN_R1576919?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/clinical-research-coordinator-5aaedc9f-9c0/

## Description

We are seeking a Clinical Research Coordinator to support study sites in the coordination of Phase I-IV clinical research studies, ensuring that studies are carried out according to protocol, standard operating procedures, GCP, and other applicable guidelines and regulations.

Key responsibilities include:

- Coordinating clinical research studies conducted by a supervising principal investigator

- Updating and maintaining skills, training and knowledge of current best nursing practice and topics related to clinical research

- Safeguarding the well-being of subjects and ensuring high standards

- Maintaining a safe environment in accordance with Health and Safety policies

- Acting as a volunteer advocate

- Dealing with volunteer and visitor concerns in a proactive manner

- Assisting staff with nursing practices and delivery of care to volunteers

- Reporting any deviations from normal practice to senior staff

- Supporting study conduct through review of study protocols, case report forms, and electronic data capture systems

- Participating in project meetings with the project team as needed

- Performing clinical set-up and preparation for studies

- Planning logistical activities for procedures

- Generating volunteer instructions

- Identifying and obtaining required supplies and equipment

- Preparing and delivering study-specific training materials, documents, and records

- Troubleshooting study issues

- Participating in huddles to ensure daily tasks are executed to expected standards

- Assisting with data quality checking and query resolution

- Recruiting and screening volunteers for inclusion in studies

- Orienting volunteers to the study and site

- Administering and maintaining custody of study drugs

- Performing complex clinical procedures, including ECGs, sample collection, spirometry, and vital signs

- Collecting, recording, and reporting clinical data and findings

- Collaborating with study investigators and monitors

Requirements:

- 1 year of relevant experience

- Good knowledge of clinical trials

- In-depth knowledge of Good Clinical Practices (GCP)

- Good skills in using MS Windows and Office applications

- Effective written and verbal communication skills

- Excellent interpersonal and problem-solving skills

- Effective organisational skills

- Ability to pay close attention to detail

- Current active nursing license in the state, country, or region where the site resides

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## Skills

### Required
- Good Clinical Practices (GCP)
- MS Windows
- Office applications
- English

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Fairfax-VA-United-States-of-America/Day-LPN_R1576919?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)