Qureos Mentor

Medix™

<div>
 
 ***Seeking a
 
 Clinical Research Coordinator in Lakewood, CO
 
 to join our clinical trials team***
 
 
 
 
 
 ✅
 
 Full Job Description:
 
 
 
 
 Position:
 
 Clinical Research Coordinator
 
 
 
 Location: Lakewood, CO
 
 
 
 
 Employment Type:
 
 Full time; Contract to Hire
 
 
 
 Pay:
 
 Up to 75k
 
 
 
 Position Overview:
 
 
 
 The research coordinator is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.
 
 
 
 
 
 
 Minimum Qualifications:
 
 
 
 &bull; Education:
 
 
 o College degree preferred or significant relevant experience
 
 
 o Ophthalmic experience preferred
 
 
 &bull; Experience / Knowledge / Skills:
 
 
 Prior annual review or promotion assessment exceeds expectations and shows high
 
 
 proficiency in the job requirements
 
 
 o Effective oral and written communication
 
 
 o Delivers safe and appropriate care to patients in addition to the requirements outlined by
 
 
 study protocols
 
 
 &bull; Certifications / Training:
 
 
 o ICH GCP Training / Certificate
 
 
 o IATA Certification
 
 
 
 
 
 
 Duties:
 
 
 
 &bull; Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study
 
 
 &bull; Administer sponsor required questionnaires (i.e. VFQ)
 
 
 &bull; Works with team member responsible for ordering study supplies (lab kits, shippers, etc.) to ensure
 
 
 adequate inventory is on hand
 
 
 &bull; Ensures study staff is properly trained on study-related information (i.e. protocol, ICF, manuals,
 
 
 etc.) and that the training is documented
 
 
 &bull; Creates, manages, and maintains source documents for each trial
 
 
 &bull; Attends teleconferences and Investigator Meetings as requested by research director
 
 
 &bull; Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections
 
 
 &bull; Works with other members of the study team and clinical team to recruit eligible candidates to meet enrollment goals
 
 
 &bull; Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility accurately
 
 
 
 Preferred Experience:
 
 
 <ul>
 <li>
 Patient-facing coordination experience.
 </li>
 <li>
 Study drug dispensing, pharmacy tech, or compounding experience a plus.
 </li>
 <li>
 Strong attention to detail and protocol compliance.
 </li>
 </ul>
 
 
 Why Join Us:
 
 
 <ul>
 <li>
 Be a key part of innovative clinical trials impacting patient care.
 </li>
 <li>
 Collaborative, mission-driven research environment.
 </li>
 <li>
 Opportunities for training and professional growth.
 </li>
 </ul>
 
 
</div>

Clinical Research Coordinator - 243120

<div>
 
 
 Job Title: Registered Nurse (RN) &ndash; Laser Treatment Specialist
 
 
 
 
 Schedule:
 
 Monday &ndash; Friday, 8:30 AM &ndash; 5:00 PM
 
 
 
 Note: Schedule subject to change
 
 
 
 
 
 
 
 Position Overview
 
 
 
 We are seeking a skilled and client-focused Registered Nurse (RN) to provide safe and effective laser treatments in a professional studio environment. This role combines clinical care with customer service, ensuring clients receive high-quality treatments while maintaining the highest standards of safety and professionalism. The ideal candidate is detail-oriented, communicative, and comfortable working directly with clients in an aesthetic treatment setting.
 
 
 
 
 
 
 Key Responsibilities
 
 
 <ul>
 <li>
 Provide safe and effective laser treatments in accordance with established treatment protocols and safety standards.
 </li>
 <li>
 Maintain accurate client documentation and ensure compliance with all treatment guidelines and regulatory requirements.
 </li>
 <li>
 Deliver excellent client-centered service by clearly explaining treatment processes, expectations, and outcomes.
 </li>
 <li>
 Build strong relationships with clients while maintaining professionalism and confidentiality.
 </li>
 <li>
 Collaborate with the studio team to achieve performance goals and contribute to a positive workplace culture.
 </li>
 <li>
 Assist with light cleaning, administrative duties, and general studio support to ensure a smooth client experience.
 </li>
 <li>
 Participate in required training and professional development opportunities.
 </li>
 <li>
 Maintain current and valid professional licensing and credentials.
 </li>
 </ul>
 
 
 
 
 
 Required Qualifications
 
 
 <ul>
 <li>
 Active New York Registered Nurse (RN) license.
 </li>
 <li>
 Reliable transportation to commute to the primary studio location.
 </li>
 <li>
 Strong communication and interpersonal skills with a client-centered approach.
 </li>
 <li>
 Ability to work flexible hours, including evenings and weekends as scheduling needs evolve.
 </li>
 <li>
 Ability to sit for extended periods (up to one hour at a time).
 </li>
 <li>
 Ability to lift 10 pounds or more repeatedly.
 </li>
 <li>
 Comfort working directly with and treating the human body in a clinical aesthetic setting.
 </li>
 <li>
 Strong wrist dexterity and hand strength to operate laser equipment and standard office equipment.
 </li>
 <li>
 Visual ability to assess client skin conditions while operating laser equipment.
 </li>
 <li>
 Ability to maintain strict confidentiality and handle sensitive information appropriately.
 </li>
 <li>
 Must meet all employment eligibility requirements.
 </li>
 </ul>
 
 
 
 
 
 Preferred Qualifications
 
 
 <ul>
 <li>
 Previous experience performing laser treatments or working in an aesthetic or dermatology setting.
 </li>
 </ul>
 
 
 
 
 
 Work Schedule
 
 
 <ul>
 <li>
 Current schedule: Monday &ndash; Friday, 8:30 AM &ndash; 5:00 PM.
 </li>
 <li>
 Schedule may change
 </li>
 </ul>
</div>

Registered Nurse - 251478

<div>
 
 A Clinical Research Coordinator (CRC) manages the daily operations of clinical trials, ensuring study protocols are followed, patient safety is maintained, and data is accurately collected. They act as the primary liaison between participants, researchers, and sponsors, handling study visits, regulatory documentation, and participant recruitment.
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 
 Participant Management:
 
 Recruit, screen, and enroll patients, obtain informed consent, and schedule study visits.
 </li>
 <li>
 
 Data Collection &amp; Entry:
 
 Accurately document study data in electronic case report forms (eCRFs) and maintain source documents.
 </li>
 <li>
 
 Protocol Adherence:
 
 Ensure all study procedures follow Good Clinical Practice (GCP) guidelines and study protocols.
 </li>
 <li>
 
 Safety Reporting:
 
 Identify and report adverse events (AEs) and serious adverse events (SAEs) promptly.
 </li>
 <li>
 
 Regulatory Documentation:
 
 Prepare and submit regulatory documents to IRBs and sponsors
 </li>
 </ul>
 
 
</div>

Clinical Research Coordinator 251215

<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

<div>
 
 
 
 *** This is an onsite role. Must be located in the Houston Texas area***
 
 
 
 
 
 
 
 
 Location:
 
 Katy, Texas &ndash; On-site
 
 
 
 Compensation:
 
 $19.00 &ndash; $22.00 / hour (Based on Experience)
 
 
 
 Schedule:
 
 Monday &ndash; Friday | 8:00 AM &ndash; 5:00 PM
 
 
 
 
 
 
 Position Overview
 
 
 
 We are seeking an experienced
 
 Medical Billing Specialist
 
 to support our medical, dental, and behavioral health billing operations. In this role, you will be the backbone of our revenue cycle, ensuring accuracy in claims submission, payment posting, and denial resolution.
 
 
 The ideal candidate thrives in a fast-paced environment, excels at navigating complex Medicaid/Medicare regulations, and takes pride in maintaining a clean AR aging report.
 
 
 
 
 
 
 Key Responsibilities
 
 
 <ul>
 <li>
 
 Claims Management:
 
 Prepare and submit accurate medical, dental, and behavioral health claims; appeal and resubmit denied/rejected claims.
 </li>
 <li>
 
 Financial Integrity:
 
 Post insurance and patient payments, process adjustments/refunds, and maintain precise accounts receivable records.
 </li>
 <li>
 
 AR Oversight:
 
 Proactively monitor AR aging reports and follow up on outstanding balances.
 </li>
 <li>
 
 Compliance:
 
 Maintain strict adherence to Medicaid, Medicare, CHIP, and HIPAA regulations.
 </li>
 <li>
 
 Reporting:
 
 Generate billing reports and identify systemic issues impacting reimbursement to share with management.
 </li>
 </ul>
 
 
 
 
 
 Required Qualifications
 
 
 <ul>
 <li>
 
 Experience:
 
 Minimum 3 years of hands-on medical billing experience.
 </li>
 <li>
 
 Education:
 
 High school diploma or equivalent.
 </li>
 <li>
 
 Technical Knowledge:
 
 Proficient in
 
 ICD, CPT, CDT, and HCPCS
 
 coding.
 </li>
 <li>
 
 Payer Expertise:
 
 Direct experience with claims submission for Medicaid, Medicare, and managed care.
 </li>
 <li>
 
 Software:
 
 Proficiency in Microsoft Office and practice management systems.
 </li>
 </ul>
 
 
 
 
 
 Preferred Qualifications
 
 
 <ul>
 <li>
 Experience within an
 
 FQHC
 
 environment.
 </li>
 <li>
 Direct experience using
 
 eClinicalWorks (eCW)
 
 .
 </li>
 <li>
 History of managing high-volume claim environments.
 </li>
 </ul>
 
 
 
 
 
 Soft Skills for Success
 
 
 <ul>
 <li>
 
 Detail-Oriented:
 
 You catch the coding errors that others miss.
 </li>
 <li>
 
 Persistent:
 
 You proactively work an account until it reaches full resolution.
 </li>
 <li>
 
 Organized:
 
 You can pivot between multiple priorities in a metric-driven environment.
 </li>
 </ul>
 
 
</div>

Medical Billing Clerk - 251091

<div>
 
 
 
 Clinical Research Assistant or Clinical Research Coordinator
 
 
 
 
 
 
 
 
 Must Haves:
 
 Must have phase 1 Oncology experience and some clinical research experience
 
 
 
 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.
 
 
 
 
 
 Purpose
 
 
 Coordinate and manage complex activities throughout the start-up, conduct, and close-out phases of clinical pharmaceutical and device research studies. Ensure timely, accurate, and objective data collection in compliance with companies Research SOPs, federal regulations, GCP, ICH guidelines, IRB requirements, and specific sponsor protocols. All work should align with company Research&rsquo;s Core Values, Mission Statement, and Employee Manual.
 
 
 
 
 
 Key Responsibilities
 
 <ul>
 <li>
 Thoroughly understand assigned protocols and ensure all patient visits and procedures are completed as specified.
 </li>
 <li>
 Accurately document patient assessments, observations, test results, and other study-related data following federal regulations and protocol requirements.
 </li>
 <li>
 Obtain informed consent from patients in compliance with federal regulations, GCP, and IRB requirements.
 </li>
 <li>
 Strategically recruit eligible study subjects to meet enrollment targets within sponsor timelines while upholding ethical and regulatory standards.
 </li>
 <li>
 Complete required training promptly.
 </li>
 <li>
 Schedule and conduct patient visits in line with protocol timelines.
 </li>
 <li>
 Maintain complete and precise source documentation for all study activities.
 </li>
 <li>
 Accurately complete and submit case report forms (CRFs/eCRFs) and sponsor worksheets.
 </li>
 <li>
 Safeguard the confidentiality of patient and study information in accordance with HIPAA, confidentiality agreements, and company policies.
 </li>
 <li>
 Promptly report adverse events to the supervisor and/or Principal Investigator/Sub-Investigator as appropriate.
 </li>
 <li>
 Notify the sponsor of Serious Adverse Events (SAEs) within 24 hours of awareness and inform the supervisor and Principal Investigator/Sub-Investigator.
 </li>
 <li>
 Manage and track study materials (e.g., study drug, CRFs, lab supplies) to ensure availability throughout the study.
 </li>
 <li>
 Maintain consistent communication and document interactions with the Team Lead I, Team Manager, Principal Investigator, Sub-Investigators, and other research staff.
 </li>
 <li>
 Participate in required training, conferences, and investigator meetings to remain current with evolving federal regulations and company policies.
 </li>
 <li>
 Continuously seek educational opportunities to deepen knowledge of clinical research processes and regulations.
 </li>
 <li>
 Perform study-related tasks efficiently and cost-effectively, always adhering to company policies.
 </li>
 <li>
 Follow safety procedures in all activities.
 </li>
 <li>
 Represent company Research professionally and courteously in all interactions&mdash;verbally, in writing, and in appearance&mdash;with patients, staff, sponsors, and external partners.
 </li>
 <li>
 Carry out additional duties as assigned by management.
 </li>
 </ul>
 
 
 
 
 Physical &amp; Environmental Requirements
 
 <ul>
 <li>
 Primarily office-based work environment.
 </li>
 <li>
 Exposure to human bodily fluids and lab processing.
 </li>
 <li>
 Direct patient care responsibilities.
 </li>
 <li>
 Daily use of computers.
 </li>
 <li>
 Occasional evening and weekend work.
 </li>
 <li>
 Ability to lift up to 35 pounds, occasionally more.
 </li>
 <li>
 Must have a valid driver&rsquo;s license and daily access to a car.
 </li>
 </ul>
 
 
 
 
 Minimum Requirements
 
 
 Education:
 
 <ul>
 <li>
 Bachelor&rsquo;s degree preferred, but not required.
 </li>
 </ul>
 
 Experience:
 
 <ul>
 <li>
 Ideally, at least 1 years in Clinical Research
 </li>
 <li>
 Oncology experience and experience with phase 1 trials is a plus
 </li>
 </ul>
 
 
 
 
 Skills &amp; Knowledge:
 
 <ul>
 <li>
 Solid understanding of clinical research methodologies.
 </li>
 <li>
 Strong leadership and team management capabilities.
 </li>
 <li>
 Effective collaboration with operational teams.
 </li>
 <li>
 Excellent verbal and written communication.
 </li>
 <li>
 Proficiency in Office 365 and other relevant software.
 </li>
 <li>
 Experience drafting and reviewing Standard Operating Procedures.
 </li>
 <li>
 Strong problem-solving, risk assessment, and analytical skills.
 </li>
 <li>
 Demonstrated process improvement experience.
 </li>
 <li>
 Effective negotiation and conflict resolution skills.
 </li>
 <li>
 Ability to multitask, prioritize tasks, and remain flexible.
 </li>
 <li>
 Independent thinker able to influence and drive decisions when needed.
 </li>
 </ul>
 
 
 
 
 
 
 
 Apply Today!
 
</div>

Clinical Research Assistant or Clinical Research Coordinator - 247968

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.