Qureos Mentor

Elite Clinical Network

<div>
 
 Position Summary
 
 
 
 The Research Assistant supports the execution of clinical research studies by performing
 
 
 administrative, technical, and participant-focused tasks under the supervision of the
 
 
 Clinical Research Coordinator and Principal Investigator. This role plays a critical part in
 
 
 ensuring high-quality data collection, regulatory compliance, and participant safety. The
 
 
 Research Assistant works collaboratively with the clinical team to facilitate study activities
 
 
 in accordance with Good Clinical Practice (GCP) guidelines, study protocols, and
 
 
 institutional policies.
 
 
 
 Key Responsibilities
 
 
 Study Support &amp; Coordination
 
 
 
 <ul>
 <li>
 Assist in preparing study materials, source documents, and regulatory binders.
 </li>
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 Support participant screening, recruitment, and scheduling in accordance with study protocols.
 </li>
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 Maintain accurate participant logs and assist in tracking enrollment progress.
 </li>
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 Ensure study areas, supplies, and equipment are organized and ready for study visits.
 
 
 </li>
 </ul>
 
 Data &amp; Documentation
 
 
 
 <ul>
 <li>
 Accurately record data from source documents into electronic case report forms (eCRFs) or databases.
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 Maintain confidentiality and integrity of participant data in compliance with HIPAA and institutional standards.
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 Assist in resolving data queries and ensuring timely data entry.
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 Support document management, filing, and archiving according to regulatory requirements.
 
 
 </li>
 </ul>
 
 Participant Interaction
 
 
 
 <ul>
 <li>
 Greet and assist study participants during visits to ensure a positive experience.
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 Prepare consent materials and provide administrative support during the informed consent process.
 </li>
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 Escort participants to appropriate testing areas and assist clinical staff with noninvasive study procedures as directed.
 
 
 </li>
 </ul>
 
 Regulatory &amp; Compliance
 
 
 
 <ul>
 <li>
 Follow Good Clinical Practice (GCP) and institutional policies at all times.
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 Support compliance with IRB, sponsor, and regulatory agency requirements.
 </li>
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 Participate in site audits, monitoring visits, and internal quality reviews as needed.
 
 
 </li>
 </ul>
 
 Team Collaboration
 
 
 
 <ul>
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 Work closely with Clinical Research Coordinators, Principal Investigators, and site teams to ensure timely completion of study milestones.
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 Participate in team meetings, training, and continuing education to stay current with study and regulatory updates.
 </li>
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 Contribute to process improvements and operational efficiency initiatives.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Associate or bachelor&rsquo;s degree in a health sciences, biology, psychology, or related field preferred.
 </li>
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 Previous experience in healthcare or research setting is strongly preferred.
 </li>
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 Familiarity with clinical trials, GCP, HIPAA, and human subjects research regulations are desirable.
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 Strong organizational, communication, and time management skills.
 </li>
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 Ability to work accurately in a fast-paced environment with strong attention to detail.
 </li>
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 Proficiency with Microsoft Office and data entry systems; experience with EDC or CTMS systems a plus.
 
 
 </li>
 </ul>
 
 Core Competencies
 
 
 
 <ul>
 <li>
 Accuracy and Attention to Detail
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 Professionalism and Confidentiality
 </li>
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 Team Collaboration
 </li>
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 Adaptability and Initiative
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 Ethical Conduct and Compliance Awareness
 
 
 </li>
 </ul>
 
 Physical Requirements
 
 
 
 <ul>
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 Ability to sit or stand for extended periods.
 </li>
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 May require occasional lifting of study materials (up to 25 lbs).
 </li>
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 Ability to interact with participants and staff in clinical and office settings.
 </li>
 </ul>
</div>

Clinical Research Assistant

<div>
 
 Job Summary
 
 
 
 We are seeking a highly organized and motivated
 
 Clinical Research Coordinator (CRC)
 
 to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling.
 
 Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred
 
 , as this role may include specimen collection and basic clinical procedures.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Coordinate day-to-day clinical research activities to ensure study protocols are followed.
 </li>
 <li>
 Recruit, screen, and enroll study participants.
 </li>
 <li>
 Obtain informed consent and ensure ethical conduct in all study interactions.
 </li>
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 Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples).
 </li>
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 Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs).
 </li>
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 Maintain accurate and timely documentation in case report forms and electronic databases.
 </li>
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 Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.
 </li>
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 Schedule participant visits and follow-ups; ensure visit windows are met.
 </li>
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 Ensure proper storage, handling, and accountability of investigational products, if applicable.
 </li>
 <li>
 Maintain regulatory documents and assist with IRB submissions.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor's degree in a health-related field or equivalent experience.
 </li>
 <li>
 At least 1&ndash;2 years of experience in clinical research preferred.
 </li>
 <li>
 Phlebotomy certification or MA certification preferred.
 </li>
 <li>
 Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
 </li>
 <li>
 Excellent organizational skills and attention to detail.
 </li>
 <li>
 Strong interpersonal and communication skills.
 </li>
 <li>
 Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms).
 </li>
 <li>
 Ability to work independently and as part of a multidisciplinary team.
 
 
 </li>
 </ul>
 
 Preferred Qualifications
 
 
 
 <ul>
 <li>
 Experience working in clinical trials, especially in a hospital or academic setting.
 </li>
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 Familiarity with IRB processes and clinical trial documentation.
 </li>
 <li>
 Bilingual skills (depending on patient population) may be a plus.
 
 
 </li>
 </ul>
 
 Job Type: Full-time
 
 
 
 
 Work Location: In person
 
 
 
 
 Schedule
 
 
 
 <ul>
 <li>
 8 hour shift
 </li>
 <li>
 Monday to Friday
 </li>
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 Weekends as needed
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 The pay rate is $20 - $30 an hour.
 </li>
 </ul>
</div>

Clinical Research Coordinator

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Clinical Research Assistant

Clinical Research Coordinator