Qureos Mentor

Medix™

<div>
 
 
 Claims Analyst &ndash; Healthcare / Insurance
 
 
 
 📍
 
 North Scottsdale, AZ (Fully Onsite to Start)
 
 
 
 💰
 
 $20 &ndash; $24 per hour
 
 
 
 🕒
 
 Flexible Schedule | 8-hour shift (start between 7:00&ndash;9:00 AM)
 
 
 
 
 
 
 About the Role
 
 
 We are seeking a detail-oriented
 
 Claims Analyst
 
 to join a rapidly growing
 
 self-funded insurance team
 
 . This role is ideal for someone who enjoys
 
 problem-solving, working with data, and navigating complex claims issues
 
 in a fast-paced environment.
 
 
 You will act as a key liaison between internal teams, brokers, and carriers&mdash;helping resolve claim discrepancies and ensuring accurate, timely processing across the full claims lifecycle.
 
 
 This team is expanding quickly, offering strong
 
 growth potential and long-term career development
 
 .
 
 
 
 
 
 Key Responsibilities
 
 <ul>
 <li>
 Investigate and resolve
 
 complex medical claims issues
 
 (denied, delayed, or incorrectly processed claims)
 </li>
 <li>
 Troubleshoot discrepancies, identify root causes, and support end-to-end claim resolution
 </li>
 <li>
 Coordinate communication across
 
 internal teams, brokers, carriers, and external partners
 
 </li>
 <li>
 Review reimbursement requests, submit claims, and follow up on outstanding payments
 </li>
 <li>
 Maintain accurate tracking logs and support claims reporting
 </li>
 <li>
 Assist with
 
 year-end reconciliation and account closure
 
 activities
 </li>
 <li>
 Ensure timely, professional communication across all stakeholders
 </li>
 <li>
 Collaborate cross-functionally to improve claims accuracy and efficiency
 </li>
 </ul>
 
 
 
 
 Required Qualifications
 
 <ul>
 <li>
 Strong
 
 Excel skills
 
 (sorting, filtering, navigating data)
 </li>
 <li>
 Experience working in a
 
 corporate or structured office environment
 
 </li>
 <li>
 Ability to learn new systems and follow structured workflows
 </li>
 <li>
 Strong attention to detail and problem-solving mindset
 </li>
 </ul>
 
 
 
 
 Preferred Qualifications
 
 <ul>
 <li>
 Healthcare or
 
 claims experience
 
 (payer-side, benefits, or processing)
 </li>
 <li>
 Experience in
 
 high-volume or fast-paced environments
 
 </li>
 <li>
 Exposure to cross-functional collaboration with internal/external partners
 </li>
 <li>
 Background in healthcare admin, medical office, or analytical roles
 </li>
 </ul>
 
 
 
 
 Schedule &amp; Work Environment
 
 <ul>
 <li>
 
 First 90 days:
 
 Fully onsite (training)
 </li>
 <li>
 
 After training:
 
 Hybrid schedule
 </li>
 <li>
 Tuesday&ndash;Thursday onsite
 </li>
 <li>
 Monday &amp; Friday remote
 </li>
 <li>
 Flexible start times between
 
 7:00 AM &ndash; 9:00 AM
 
 </li>
 </ul>
 
 
 
 
 Why Join This Team?
 
 
 ✨
 
 Hybrid flexibility
 
 after training
 
 
 📈
 
 High-growth team
 
 with advancement opportunities
 
 
 💰
 
 Performance-based bonus program
 
 
 
 🏥
 
 Comprehensive benefits starting Day 1
 
 
 
 🌴 Generous PTO + paid company holidays
 
 
 📚 Collaborative, learning-focused environment
 
</div>

Claims Specialist - 253047

<div>
 
 
 Job Title:
 
 Clinical Research Coordinator
 
 
 
 
 
 
 Location
 
 : Cincinnati, OH
 
 
 
 
 
 
 Position Type
 
 : This is a
 
 Contract Opportunity -
 
 the contract would be expected to be about 3 months (90 days from the candidate start date). At the time they pass the 90 day mark the employer would conduct a candidate performance review, as well as a review of the site's needs at the time. There is a potential for the contract to be extended depending on project needs at the time, or to be brought on permanently with the employer. (NOT guaranteed and NOT planned at this time)
 
 
 
 
 
 
 Job Summary:
 
 
 
 The Clinical Research Coordinator conducts and manages clinical trials in accordance with the study protocol, GCP, and company SOPs.
 
 
 
 
 
 
 Duties/Responsibilities:
 
 
 <ul>
 <li>
 Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and company SOPs
 </li>
 <li>
 Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.
 </li>
 <li>
 Implement research and administrative strategies to successfully manage assigned protocols.
 </li>
 <li>
 Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
 </li>
 <li>
 Apply good documentation practices when collecting and correcting data, transferring data to sponsor/CRO data capture systems, and resolving queries
 </li>
 <li>
 Maintain confidentiality of patient protected health information, sponsor confidential information and company confidential information
 </li>
 <li>
 Ensure patient safety is upheld and all adverse events, serious adverse events, and adverse events of special interest are followed and reported in accordance with the protocol and company SOPs.
 </li>
 <li>
 Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner
 </li>
 <li>
 Ensure staff are delegated and trained appropriately and documented
 </li>
 <li>
 Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
 </li>
 <li>
 Evaluate potential subjects for participation in clinical trials including phone and in person prescreens.
 </li>
 <li>
 Execute recruitment strategies defined by Clinical Research Team
 </li>
 <li>
 Understand key timelines, endpoints, required vendors, and patient population for each assigned protocol.
 </li>
 <li>
 Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope
 </li>
 <li>
 Promote respect for cultural diversity and conventions with all individuals.
 </li>
 </ul>
 
 
 
 
 
 Education/Experience:
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree with 1 year of relevant experience in the life science industry OR
 </li>
 <li>
 Associate&rsquo;s degree with 2 years of relevant experience in the life science industry OR
 </li>
 <li>
 High School Graduate and/or technical degree with minimum of 3 years relevant experience in the
 </li>
 <li>
 life science industry
 </li>
 </ul>
 
 
 
 
 
 Required Licenses/Certifications:
 
 
 <ul>
 <li>
 Phlebotomy if applicable and required by state law
 </li>
 <li>
 Intramuscular dose administration and preparation if applicable and required by state law
 </li>
 </ul>
 
 
 
 
 
 Required Skills:
 
 
 <ul>
 <li>
 Demonstrated knowledge of medical terminology
 </li>
 <li>
 Demonstrated ability in the use of the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
 </li>
 <li>
 Demonstrated ability to work in a fast-paced environment
 </li>
 <li>
 Demonstrated verbal, written, and organizational skills
 </li>
 <li>
 Demonstrated interpersonal and communication skills
 </li>
 <li>
 Demonstrated ability to work as a team player
 </li>
 <li>
 Demonstrated ability to read, write, and speak English
 </li>
 <li>
 Demonstrated ability to multi-task
 </li>
 <li>
 Demonstrated ability to follow written guidelines
 </li>
 <li>
 Demonstrated ability to work independently, plan and prioritize with some guidance
 </li>
 <li>
 Demonstrated ability to be flexible/adapt as daily schedule may change rapidly
 </li>
 <li>
 Must be detail oriented
 </li>
 <li>
 Demonstrated problem solving and strategic decision making ability.
 </li>
 <li>
 Proficient ability to accept individual responsibility for actions taken and demonstrate professionalism when judged, critiqued and/or praised.
 </li>
 </ul>
 
 
 
 
 
 Required Physical Abilities:
 
 
 <ul>
 <li>
 Sit or stand for long periods of time
 </li>
 <li>
 Travel locally and nationally
 </li>
 <li>
 Communicate in person and by a telephone
 </li>
 <li>
 Limited walking required
 </li>
 <li>
 Limited to lifting up to 30 pounds
 </li>
 </ul>
 
 
 
 
 NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.
 
</div>

Clinical Research Coordinator - 251960

<div>
 
 
 
 Clinical Research Assistant
 
 
 
 
 
 
 
 
 Must Haves:
 
 Must have experience as a Clinical Research Assistant, and experience with Oncology
 
 
 
 Hours:
 
 40 hours per week, Monday-Friday, onsite, normal business hours. Need someone flexible to come in earlier or stay later for patient needs.
 
 
 
 Contract Duration:
 
 Permanent position
 
 
 
 Benefits:
 
 Medical, Dental, Vision, time off, paid holidays off, bonus, 401k, growth opportunities, etc.
 
 
 
 
 
 
 Responsibilities
 
 
 
 
 
 
 The Research Assistant I is an essential team member in the conduct and execution of clinical research studies. The Research Assistant is to assist under direct supervision of the Site Director or Clinical Research Coordinator (CRC) in clinic supporting activities and perform duties and procedures related to the start-up, conduct and close-out phases of clinical research protocols. Under direct supervision and direction, to help obtain clean, objective, and accurate data within provided timelines while following applicable federal regulations, medical ethics, Good Clinical Practices (GCPs), Institutional Review Board (IRB) requirements, and in compliance with specific sponsor protocol requirements. All responsibilities should be completed in accordance with the companies Mission Statement and Employee Manual.
 
 
 
 
 
 
 Required Skills
 
 
 
 
 
 <ul>
 <li>
 
 Education:
 
 Associate in Science degree or adequate experience within the field of clinical research to compensate. Bachelor's degree preferred.
 </li>
 <li>
 
 Experience:
 
 Preferably a
 
 
 minimum of 1-3+ years&rsquo; experience within the field of clinical research or biological research. Must have experience with Oncology.
 </li>
 </ul>
 
 
 
 
 
 Preferred Skills
 
 
 
 
 
 <ul>
 <li>
 Exceptional knowledge of clinical research methods.
 </li>
 <li>
 Demonstrates core values &amp; all skills set required.
 </li>
 <li>
 Demonstrated ability to collaborate and align with all research department teams.
 </li>
 <li>
 Excellent oral and written communication skills.
 </li>
 <li>
 Excellent computer skills to include Office365 products.
 </li>
 <li>
 Is moral and ethical in decision-making and during interaction with patients, sponsor and IRB representatives, physicians and staff at satellite clinics, and other employees.
 </li>
 <li>
 Must be professional, have a strong work ethic, be motivated to identify tasks that need to be completed and to strive for accuracy and quality when completing assignments.
 </li>
 <li>
 ECG, phlebotomy skills, and any other technical skills related to the completion of a study visit as required by the protocol.
 </li>
 <li>
 Must be able to adapt and take on additional tasks as requested.
 </li>
 <li>
 Assists with key initiatives/process improvements in the department.
 </li>
 <li>
 Assists with training company new hires.
 </li>
 <li>
 Completes at least 80% of goals annually.
 </li>
 </ul>
 
 
 
 
 
 
 
 Apply Today!
 
</div>

Clinical Research Assistant - 251480

<div>
 
 The Clinical Research Coordinator (CRC) is responsible for the daily management and execution of clinical trials at the research site, working under the guidance of the Principal Investigator (PI). The CRC ensures that studies are conducted in accordance with the study protocol, ICH-GCP guidelines, FDA regulations, and institutional SOPs. The CRC acts as a liaison between the PI, study participants, sponsors, and the Institutional Review Board (IRB) to ensure participant safety and data integrity.
 
 
 Key Responsibilities
 
 <ul>
 <li>
 
 Study Startup &amp; Regulatory:
 
 Assist with protocol review, IRB submissions, and preparation of regulatory binders.
 </li>
 <li>
 
 Participant Recruitment &amp; Screening:
 
 Identify, recruit, and screen potential participants against inclusion/exclusion criteria.
 </li>
 <li>
 
 Informed Consent:
 
 Conduct the informed consent process, ensuring participants understand study requirements, risks, and benefits.
 </li>
 <li>
 
 Study Visits &amp; Procedures:
 
 Coordinate and conduct study visits, perform study procedures (e.g., ECGs, vitals), and manage participant follow-up.
 </li>
 <li>
 
 Data Management:
 
 Collect, record, and enter accurate source data into Electronic Data Capture (EDC) systems in a timely manner; resolve queries.
 </li>
 <li>
 
 Specimen Management:
 
 Collect, process, label, store, and ship laboratory specimens according to the protocol and IATA regulations.
 </li>
 <li>
 
 Safety &amp; Compliance:
 
 Monitor participant safety, record adverse events (AEs), and report serious adverse events (SAEs) promptly to the PI and sponsor.
 </li>
 <li>
 
 Investigational Product (IP):
 
 Oversee proper receipt, storage, dispensing, and accountability of study drugs/devices.
 </li>
 <li>
 
 Site Visits:
 
 Host sponsor monitoring visits
 </li>
 </ul>
 
 
</div>

Clinical Research Coordinator 252387

Clinical Research Coordinator  252171

<div>
 
 
 Title:
 
 Bilingual Nurse Practitioner / Physician Assistant (Polish/English) &ndash; Oncology
 
 
 
 
 
 
 Summary:
 
 
 
 We are seeking a
 
 Bilingual Nurse Practitioner / Physician Assistant (Polish/English)
 
 to join a collaborative clinical team supporting multiple physicians in an oncology practice. This role focuses on providing follow-up care to patients undergoing treatment and supporting physicians in delivering high-quality, patient-centered care. The ideal candidate is confident in clinical decision-making, reliable, and passionate about providing compassionate care to patients and their families.
 
 
 
 
 
 
 Day to Day:
 
 
 <ul>
 <li>
 See approximately
 
 15&ndash;20 patients per day
 
 , primarily for follow-up visits
 </li>
 <li>
 Assess, plan, implement, and evaluate patient care plans
 </li>
 <li>
 Document patient care, interventions, and outcomes in the medical record
 </li>
 <li>
 Educate patients and families on treatment plans, care management, and wellness strategies
 </li>
 <li>
 Perform procedures after appropriate training
 </li>
 <li>
 Collaborate closely with physicians and clinical staff to ensure coordinated care
 </li>
 <li>
 Identify patient and family needs and connect them with appropriate resources
 </li>
 <li>
 Maintain timely documentation and ensure compliance with regulatory standards
 </li>
 <li>
 Participate in patient care management and support clinical best practices
 </li>
 </ul>
 
 
 
 
 
 Qualifications:
 
 
 <ul>
 <li>
 
 Bilingual:
 
 Polish and English
 </li>
 <li>
 
 Current Nurse Practitioner licensure
 
 </li>
 <li>
 
 BLS/CPR certification
 
 </li>
 <li>
 
 At least 1 year of clinical experience
 
 </li>
 <li>
 Strong communication skills and ability to work collaboratively with physicians and care teams
 </li>
 </ul>
 
 
 
 
 
 Perks!:
 
 
 <ul>
 <li>
 Opportunity to work closely with experienced physicians
 </li>
 <li>
 Supportive and collaborative clinical environment
 </li>
 <li>
 Consistent weekday schedule
 </li>
 <li>
 Ability to build strong patient relationships and make a direct impact on patient care
 </li>
 </ul>
 
 
 
 
 
 Shift:
 
 
 <ul>
 <li>
 Monday &ndash; Friday
 </li>
 <li>
 8:00 AM &ndash; 4:30 PM
 
 or
 
 8:30 AM &ndash; 5:00 PM
 </li>
 </ul>
 
 
</div>

Nurse Practitioner / Physician Assistant - 251424

Join Medix™ and explore 6   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.