Qureos Mentor

Medix™

<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>
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 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.
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 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>
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 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

<div>
 
 
 
 Role
 
 
 : Clinical Research Coordinator - 3 month Contract assignment, 30 hours a week
 
 
 
 
 
 
 
 
 
 
 Location
 
 
 : Onsite - Leesburg, VA 20176
 
 <ul>
 <li>
 Relocation candidates will NOT be considered for this position
 </li>
 <li>
 Role is
 
 100% onsite,
 
 there is no opportunity for hybrid or remote work at this time
 </li>
 </ul>
 
 
 
 
 
 
 
 
 
 Therapeutic Area
 
 
 
 :
 
 Cardiology
 
 
 
 
 
 
 
 
 
 
 Employment Type
 
 
 : Position is a contract, project based support role - current contract duration is estimated to be 3 months, possibility for extension depending on project needs
 
 
 
 
 
 
 
 
 
 
 Schedule/ Shift:
 
 
 
 <ul>
 <li>
 30 hours a week
 </li>
 <li>
 M-F during daytime business hours - NO evenings/weekends, open to reviewing candidates' preferred schedules
 </li>
 </ul>
 
 
 
 
 
 
 
 
 
 Responsibilities/ Job Duties:
 
 
 
 
 We are seeking a detail-oriented Clinical Research Coordinator (CRC) with a strong focus on data management and electronic data capture (EDC) to support the successful execution of clinical trials. This role is ideal for candidates who excel in data entry, data quality review, and working within multiple EDC systems in a fast-paced research environment.
 
 
 
 
 
 The CRC will be responsible for:
 
 <ul>
 <li>
 Accurate and timely data entry, query resolution, and ongoing data maintenance across clinical trial platforms.
 </li>
 <li>
 Candidates should bring hands-on experience with a variety of EDC systems&mdash;such as Medidata Rave, Oracle InForm, Oracle Clinical, Veeva Vault, or similar&mdash;demonstrating adaptability and fluency across platforms.
 </li>
 <li>
 Experience limited to a single system (e.g., REDCap only) will not be sufficient for this role.
 </li>
 </ul>
 
 
 
 
 This position plays a critical role in ensuring data integrity, protocol compliance, and audit readiness, while collaborating closely with study teams, sponsors, and site staff. The ideal candidate is highly organized, proactive, and committed to maintaining the highest standards of clinical research data quality.
 
</div>

Clinical Research Coordinator - 250730

<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
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 <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 4   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

Clinical Research Assistant - 251480

Clinical Research Coordinator 252387

Clinical Research Coordinator - 250730

Nurse Practitioner / Physician Assistant - 251424