Clinical Quality Coordinator DelRicht Research - 3.4 New Orleans, LA Job Details Temporary | Full-time $50,000 - $60,000 a year 15 hours ago Qualifications Optimizing workflow processes Data integrity assurance Google Sheets Clinical research Clinical compliance checks Data validation techniques Bachelor of Science Data quality management Data integrity and documentation Continuous improvement Health information data integrity Team training Clinical information systems Quality control Quality improvement Computer skills Manual chart audits Medical terminology Bachelor of Arts Communication skills Entry level Cross-functional communication Under 1 year Time management Quality assurance experience within healthcare Full Job Description Play a Key Role in Clinical Research - Temporary, Full Time Role in Metairie! Looking for a short-term position in healthcare, medicine, or clinical research? Help us move medicine forward by playing an active role in conducting new and innovative clinical trials in your community. DelRicht Research is an integrated organization of premier investigational sites. Our mission is to move medicine forward by providing the best quality service to our clients and engaging more patients in clinical research. This is a full-time, temporary role projected to last 6-8 weeks, with the potential for extension or conversion to a permanent role. No prior clinical research experience required- just bring your attention to detail, curiosity, and enthusiasm!

NOTE:

This is an onsite M-F position based at our Corporate Headquarters location in Metairie, LA.

Clinical Quality Coordinator's Main Objective:

This role is responsible for supporting the Quality Assurance (QA) team with process improvement initiatives, as well as training, and trend identification across the site network's clinics. The Clinical Quality Coordinator will maintain clinical trial data integrity to ensure site is audit ready at all times. The Clinical Quality Coordinator will assist with oversight and maintenance of activities related to the conduct of clinical trials at the site including but not limited to: Complete chart reviews to ensure consistency and accuracy across our electronic medical record (EMR) platforms Ensure compliance with clinical trial protocols Coordinate, communicate and collaborate with clinical teams across our site network Detail plans for timely correction of electronic source errors Skills needed to win: B.S or B.A from any accredited university in any degree Proficiency with Google Sheets, Excel, and other cloud-based computer systems

Preferred:

1 year of healthcare experience; confidence reviewing medical charts, medical terminology, and healthcare operations The right candidate will: Be self motivated, energetic and positive Be a team player with excellent communication skills Ability to work autonomously, with strong organizations and effective time management skills Be skilled at problem solving and solution focused Coffee drinkers preferred. Tea drinkers accepted.

DelRicht Research's Core Values:

Production, Humility, Consistency Production:

Production :

We deliver on our promises, take action, and solve problems proactively.

Humility :

We support each other, bring enthusiasm, and embrace change.

Consistency :

We value accuracy, persistence, and staying calm under pressure.

Compensation Range :

$50,000-$60,000

Job Type :

Temporary (4-6 months), full time

Working Hours :

Monday-Friday, 8am-5pm

Working Location :

On-site in Metairie, Louisiana Visit our website linked to learn about our company and current clinical trials, see patient testimonials, and check out our careers page! We are an equal opportunity employer and consider all qualified applicants equally without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.