Qureos Mentor

Medix™

<div>
 
 
 
 Senior Clinical Research Coordinator
 
 
 
 
 
 
 
 
 Must Haves:
 
 Must have 3-5 years of CRC experience, some sort of managerial experience within clinical research is preferred
 
 
 
 Hours:
 
 40 hours per week, Monday-Friday 9am-5pm, fully onsite
 
 
 
 Contract Duration:
 
 Permanent position
 
 
 
 Benefits:
 
 Medical, Dental, Vision, time off, paid holidays off, bonus. 401k, growth opportunities, etc.
 
 
 
 
 
 
 PURPOSE:
 
 
 
 To coordinate a variety of complex activities and perform duties and procedures related to the start-up, conduct and close-out phases of clinical pharmaceutical and device research protocols. To obtain clean, objective, and accurate data within sponsor timelines while following applicable company SOPs, policies and procedures, federal regulations, medical ethics, Good Clinical Practices (GCPs), International Council of Harmonization (ICH), Institutional Review Board (IRB) requirements, and in compliance with specific sponsor protocol requirements. All responsibilities should be completed in accordance with the companies Core Values, Mission Statement and Employee Manual.
 
 
 
 
 
 
 ESSENTIAL JOB FUNCTIONS:
 
 
 <ul>
 <li>
 Read, understand, and can accomplish protocol specified patient visits and procedures.
 </li>
 <li>
 Clearly and concisely document patient assessments, observations, test results and other study related information per federal regulations, protocol requirements and GCPs.
 </li>
 <li>
 Obtain patient informed consent according to federal regulations, GCPs and IRB requirements.
 </li>
 <li>
 Is creative and diligent in recruiting qualified study subjects into assigned protocols to fulfill enrollment obligations within the sponsor&rsquo;s timeline while following regulations and rules governing medical ethics, IRB, GCP and ICH guidelines.
 </li>
 <li>
 Complete all required training in a timely manner.
 </li>
 <li>
 Schedule and conduct patient visits according to protocol requirements and timelines.
 </li>
 <li>
 Maintain accurate and complete written source documentation of patient visits and protocol related activities.
 </li>
 <li>
 Accurately complete case report forms (CRFs &amp;/or eCRFs) and/or worksheets generated by the sponsor.
 </li>
 <li>
 Maintain confidentiality of patient and protocol issues as appropriate and as bound by Confidentiality Agreements with company, between company and sponsors, and between company and other entities, as well as HIPAA regulations.
 </li>
 <li>
 Promptly report adverse events to supervisor and/or Principal Investigator/Sub-Investigator as deemed necessary.
 </li>
 <li>
 Report Serious Adverse Events (SAEs) to sponsor within 24 hours of becoming aware of the SAE. Also report the SAE to the supervisor, Principal Investigator and/or Sub-Investigator.
 </li>
 <li>
 Account for clinical trial materials (i.e., CRFs, study drug, lab supplies, and/or other required items) and ensure availability of appropriate amounts for the conduct of the study.
 </li>
 <li>
 Maintain ongoing communication with team manager; Principal Investigator; Sub-Investigators and other persons assisting with the trial and document these communications according to protocol requirements and company policies.
 </li>
 <li>
 Attend required training courses/conferences in order to stay abreast of current and changing federal regulations and company policies.
 </li>
 <li>
 Pursue educational opportunities to increase knowledge of the research process and associated rules and regulations governing clinical research.
 </li>
 <li>
 Attend Investigator Meetings and/or other trainings as directed.
 </li>
 <li>
 Perform all study-related duties in a time- and cost-effective manner in adherence with company policies.
 </li>
 <li>
 Represent the company in a professional and courteous manner (verbal, written and in appearance) when interacting with company staff, sponsors, IRBs, patients/subjects, nursing and medical staff members of various clinics, hospitals, and physician&rsquo;s offices.
 </li>
 <li>
 Additional duties as assigned by management.
 </li>
 </ul>
 
 
 
 
 
 PHYSICAL REQUIREMENTS AND/OR ENVIRONMENTAL FACTORS:
 
 
 <ul>
 <li>
 Work is normally performed in a typical interior/office work environment.
 </li>
 <li>
 Travel may be required for conferences and/or training.
 </li>
 <li>
 Exposure to human bodily fluids.
 </li>
 <li>
 Laboratory processing procedures.
 </li>
 <li>
 Subject/Patient care.
 </li>
 <li>
 Daily computer use.
 </li>
 <li>
 Occasional night and weekend work schedules depending on study requirements.
 </li>
 <li>
 The ability to properly lift thirty-five pounds and occasionally more than thirty-five pounds.
 </li>
 <li>
 Ability to drive, and daily availability of an automobile.
 </li>
 </ul>
 
 
 
 
 
 MINIMUM REQUIREMENTS:
 
 
 
 
 Education:
 
 Bachelor's degree preferred; however, is not required.
 
 <ul>
 <li>
 
 Experience:
 
 Preferably a minimum of 3 years&rsquo; experience as a CRC, plus 5+ years' minimum experience within the field of clinical research or biological research. Some sort of management experience preferred.
 </li>
 </ul>
 
 
 
 
 
 
 
 Apply Today!
 
</div>

Senior Clinical Research Coordinator - 247540

<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>
 
 
 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 3   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.

Medix™

About Company

Senior Clinical Research Coordinator - 247540

Clinical Research Assistant - 251480

Nurse Practitioner / Physician Assistant - 251424