Clinical Quality Program Coordinator
Company: Delricht Research
Location: New Orleans
Posted on: April 1, 2026
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Job Description:
Why DelRicht Research? Would you love to be a part of the
cutting edge of healthcare and science innovation? Are you looking
for a position that has sustainable opportunities for professional
growth? We are a clinical research company dedicated to providing
an excellent customer experience to all patients that participate
in our clinical trials. Our clinical trials provide new treatment
options for our patients and, ultimately, our goal is to get new
medications and medical devices FDA approved. We are currently
looking for a detail-oriented, confident Clinical Quality Program
Coordinator to join our team. DelRicht Research has been recognized
as one of New Orleans Top Workplaces for 2023, 2024, and 2025! This
is a testament to our unwavering commitment to creating an
exceptional work environment that fosters growth, collaboration,
and employee satisfaction. NOTE: This is an onsite M-F position
based at our New Orleans Corporate Headquarters location. Who We
Are DelRicht is a clinical research company dedicated to providing
an excellent customer experience to all patients that participate
in our clinical trials. Our clinical trials provide new treatment
options for our patients and ultimately our goal is to get new
medications FDA approved! We hold our team members to a high
standard of excellence and are looking for energetic, positive,
quick learners to be a part of our team. Presently our network
stretches across 18 sites throughout the United States. Clinical
Quality Program 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 Program Coordinator will maintain clinical trial data
integrity to ensure site is audit ready at all times. The Clinical
Quality Program 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 Quality
Assurance (QA) chart reviews, ensuring consistency, accuracy, and
timeliness Ensure that clinical trial protocols are being adhered
to 100% of the time Coordinate, communicate and collaborate with
clinical teams across our site network Maintain a working knowledge
of FDA regulations, GCP/ICH guidelines, organizational SOPs,
guidance documents and study protocols Detail plans for timely
correction of electronic source errors Ensure both inter- and
intra-site consistency in source completion Manage and report
charting trends to leadership Assist with training for both
clinical teams and the QA department Assist the QA manager with
internal team training, developing and disseminating reports, and
management tasks related to QA Coordinators The right candidate
will: Required: Minimum 3 years of professional work experience
Required: B.S or B.A from any accredited university in any degree
Required: Experience in a clinic, quality assurance, project
management, or similar healthcare environment Required: Familiarity
with medical intake and terminology, Required: Experience with
quality assurance (does not have to be in healthcare) Preferred :
Experience working within cross-functional teams on process
improvement initiatives Preferred : Familiarity with clinical
charting and clinical reports. Be self motivated, energetic and
positive Be a team player with excellent communication skills Be
comfortable speaking to external and internal stakeholders and
leaders Ability to work autonomously with a high level of self
accountability Make sure client satisfaction is a primary focus and
that the client is able to achieve and exceed their goals Believe
in high quality and have a high standard of compliance to our study
protocols Be remarkably organized with effective time management
skills Be skilled at problem solving and solution focused Manage
multiple tasks and clinical trials efficiently Accept ownership of
tasks from inception through completion and assume responsibility
for personal success Coffee drinkers preferred. Tea drinkers
accepted. DelRicht Research’s Core Values: Production, Humility,
Consistency Production : We deliver on our promises We have a bias
towards action: we value independent problem solving We proactively
over deliver: we can act without being told what to do and we
always have new ideas that will be heard and will improve the
company Humility : We support each other relentlessly We always
have enthusiasm: we exhibit passion and excitement about our work
which leads to everyone having a ‘can do’ attitude We embrace
change: we are excited to always be growing and moving the
organization forward which means change is the norm for us
Coachable: we all love to learn, we are willing to be taught and
will adapt quickly Consistency : We always are able to execute: we
get it right the first time and promote ‘touch it once’ accuracy We
have persistence: we demonstrate the tenacity and willingness to go
the distance to get something done We are calm under pressure: we
can maintain stable performance when under heavy pressure or stress
Our team comes first so here are some of the perks and benefits at
DelRicht Research: Comprehensive benefits - medical, dental &
vision Generous Paid Time Off that builds throughout your career
with the company Even though we are in healthcare, we do not work
nights, weekends or long day shifts (yes nurses love us) 401K
(including discretionary match/profit sharing) Exceptional
quarterly bonus plan that clearly outlines your bonus potential per
quarter and giving the team the visibility and control to maximize
earnings by hitting team goals Visit our website linked below to
learn about our company and current clinical trials, see patient
testimonials, and check out our careers page! Website :
www.delrichtresearch.com Patient Testimonials :
https://delrichtresearch.com/testimonials/
Keywords: Delricht Research, New Orleans , Clinical Quality Program Coordinator, Science, Research & Development , New Orleans, Louisiana