Qureos Mentor

DelRicht Research

<div>Why DelRicht Research?

Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a position that has sustainable opportunity for professional growth? If the answer is yes, then DelRicht Research might be the right opportunity for you! 

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 and medical devices 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 33 sites throughout the United States in 18 states. 

DelRicht Research has been recognized as a Top Workplace 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. 

Clinical Research Coordinator&rsquo;s Main Objective: Overall, the Clinical Research Coordinator is responsible for providing quality, excellent patient care and a great experience for our patients in our clinical research studies: 
<ul>
<li>Patients have a fun, positive and comfortable experience at our clinic</li>
<li>Patient visits are completed accurately and efficiently seeing to it that all clinical trial protocols are being adhered to 100% of the time</li>
<li>Patient recruitment and enrollment into clinical trials</li>
<li>Administer intramuscular injections (IMs) safely and accurately</li>
<li>Ensuring patients come to and complete their clinical trial visits throughout the study</li>
<li>Data Entry timely and accurately entered for clinical visits into multiple online systems</li>
<li>Lead and main point of contact for Pharmaceutical Sponsors and Contract Research Organizations for all clinical trials</li>
<li>Ensuring Sponsors and Clients have amazing customer service when they are onsite at our clinic and assuring we are always providing clear, constant communication with them when they are off site</li>
<li>Maintaining Physician Trust - You are seen as a go to, knowledgeable resource to our physicians including ensuring the physician is well informed of their schedule and updated on all current clinical trial patients and protocols</li></ul> 
 
Skills needed to win: 
<ul>
<li>Required: Minimum of 3 years of professional experience</li>
<li>Required: Active Registered Medical Assistant (RMA), Certified Medical Assistant (CMA), Licensed Practical Nurse (LPN), or Registered Nurse (RN) certification</li>
<li>Preferred: B.S or B.A from any accredited university</li>
<li>This is an onsite Monday-Friday position. 
</li>
<li>Coffee drinkers preferred. Tea drinkers accepted.</li></ul> 
 
The Right Candidate Will:
<ul>
<li>Be self motivated! Energetic! Positive!</li>
</ul><ul><li>Focus on providing exceptional patient care and creating memorable experiences</li>
</ul><ul><li>Make sure client satisfaction is a primary focus and that the client is able to achieve and exceed their goals</li>
</ul><ul><li>Believe in high quality and have a high standard of compliance to our study protocols</li>
</ul><ul><li>Be remarkably organized</li>
</ul><ul><li>Be skilled at problem solving, planning and being proactive</li>
<li>Accept ownership of tasks from inception through completion and assume responsibility for personal success</li></ul> 
 
DelRicht Research&rsquo;s Core Values: Production, Humility, Consistency

Production:
<ul>
<li>We deliver on our promises</li>
<li>We have a bias towards action: we value independent problem solving</li>
<li>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</li> 
</ul>
Humility:
<ul>
<li>We support each other relentlessly</li>
<li>We always have enthusiasm: we exhibit passion and excitement about our work which leads to everyone having a &lsquo;can do&rsquo; attitude</li>
<li>We embrace change: we are excited to always be growing and moving the organization forward which means change is the norm for us</li>
<li>Coachable: we all love to learn, we are willing to be taught and will adapt quickly</li> 
</ul>
Consistency:
<ul>
<li>We always are able to execute: we get it right the first time and promote &lsquo;touch it once&rsquo; accuracy</li>
<li>We have persistence: we demonstrate the tenacity and willingness to go the distance to get something done</li>
<li>We are calm under pressure: we can maintain stable performance when under heavy pressure or stress</li></ul> 


Team Perks &amp; Benefits at DelRicht Research:
<ul>
<li>Medical Insurance, with generous employer paid contributions</li>
<li>Dental and Vision Insurance</li>
<li>Short and Long Term Disability and Group Life Coverage</li>
<li>Paid Time Off that builds throughout your career with the company</li>
<li>401K (+ discretionary match/profit sharing)</li>
<li>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</li>
<li>Professional Development Program tailored to each team member&rsquo;s profess goals. Our quarterly goal-setting initiative is designed to challenge our team members to reach and exceed their potential!</li>
<li>Success-Driven Environment where data drives our decisions and insights. Be a part of a winning team that prioritizes transparency, continuous improvement, and success!</li> 
</ul>
Job Type: Full-Time 40+ hrs 
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/ 

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.</div>

Clinical Research Coordinator (Medical Assistant Certification Required!)

<div>
 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 Documentation Specialist 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 Documentation Specialist&rsquo;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&rsquo;s clinics. The Clinical Documentation Specialist will maintain clinical trial data integrity to ensure site is audit ready at all times
 
 
 The Clinical Documentation Specialist Will Assist With Oversight And Maintenance Of Activities Related To The Conduct Of Clinical Trials At The Site Including But Not Limited To
 
 
 <ul>
 <li>
 Complete Quality Assurance (QA) chart reviews, ensuring consistency, accuracy, and timeliness
 </li>
 <li>
 Ensure that clinical trial protocols are being adhered to 100% of the time
 </li>
 <li>
 Coordinate, communicate and collaborate with clinical teams across our site network
 </li>
 <li>
 Maintain a working knowledge of FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents and study protocols
 </li>
 <li>
 Detail plans for timely correction of electronic source errors
 </li>
 <li>
 Ensure both inter- and intra-site consistency in source completion
 </li>
 <li>
 Manage and report charting trends to leadership
 </li>
 <li>
 Assist with training for both clinical teams and the QA department
 </li>
 <li>
 Assist the QA manager with internal team training, developing and disseminating reports, and management tasks related to QA Coordinators
 
 
 </li>
 </ul>
 
 The Right Candidate Will
 
 
 
 <ul>
 <li>
 Required: Minimum 3 years of professional work experience
 </li>
 <li>
 Required: B.S or B.A from any accredited university in any degree
 </li>
 <li>
 Required: Experience in a clinic, quality assurance, project management, or similar healthcare environment
 </li>
 <li>
 Required: Familiarity with medical intake and terminology.
 </li>
 <li>
 Required: Experience with quality assurance (does not have to be in healthcare)
 </li>
 <li>
 Preferred: Experience working within cross-functional teams on process improvement initiatives
 </li>
 <li>
 Preferred: Familiarity with clinical charting and clinical reports.
 </li>
 <li>
 Be self motivated, energetic and positive
 </li>
 <li>
 Be a team player with excellent communication skills
 </li>
 <li>
 Be comfortable speaking to external and internal stakeholders and leaders
 </li>
 <li>
 Ability to work autonomously with a high level of self accountability
 </li>
 <li>
 Make sure client satisfaction is a primary focus and that the client is able to achieve and exceed their goals
 </li>
 <li>
 Believe in high quality and have a high standard of compliance to our study protocols
 </li>
 <li>
 Be remarkably organized with effective time management skills
 </li>
 <li>
 Be skilled at problem solving and solution focused
 </li>
 <li>
 Manage multiple tasks and clinical trials efficiently
 </li>
 <li>
 Accept ownership of tasks from inception through completion and assume responsibility for personal success
 </li>
 <li>
 Coffee drinkers preferred. Tea drinkers accepted.
 
 
 </li>
 </ul>
 DelRicht Research&rsquo;s Core Values: Production, Humility, Consistency
 
 
 
 Production
 
 
 
 <ul>
 <li>
 We deliver on our promises
 </li>
 <li>
 We have a bias towards action: we value independent problem solving
 </li>
 <li>
 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
 
 
 </li>
 </ul>
 
 Humility
 
 
 
 <ul>
 <li>
 We support each other relentlessly
 </li>
 <li>
 We always have enthusiasm: we exhibit passion and excitement about our work which leads to everyone having a &lsquo;can do&rsquo; attitude
 </li>
 <li>
 We embrace change: we are excited to always be growing and moving the organization forward which means change is the norm for us
 </li>
 <li>
 Coachable: we all love to learn, we are willing to be taught and will adapt quickly
 
 
 </li>
 </ul>
 
 Consistency
 
 
 
 <ul>
 <li>
 We always are able to execute: we get it right the first time and promote &lsquo;touch it once&rsquo; accuracy
 </li>
 <li>
 We have persistence: we demonstrate the tenacity and willingness to go the distance to get something done
 </li>
 <li>
 We are calm under pressure: we can maintain stable performance when under heavy pressure or stress
 
 
 </li>
 </ul>
 Our team comes first so here are some of the perks and benefits at DelRicht Research:
 
 
 <ul>
 <li>
 Comprehensive benefits - medical, dental &amp; vision
 </li>
 <li>
 Generous Paid Time Off that builds throughout your career with the company
 </li>
 <li>
 Even though we are in healthcare, we do not work nights, weekends or long day shifts (yes nurses love us)
 </li>
 <li>
 401K (including discretionary match/profit sharing)
 </li>
 <li>
 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
 
 
 </li>
 </ul>
 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/
</div>

Clinical Documentation Specialist

Join DelRicht Research and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

DelRicht Research

About Company

Clinical Research Coordinator (Medical Assistant Certification Required!)

Clinical Documentation Specialist