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The role will require the desire to learn and grow rapidly, and include the opportunity to work closely with Topography&#39;s partner healthcare groups.</p>\n<p>Key responsibilities include acting as a research assistant to clinical trials conducted within physician practices, visit preparation activities, visit follow-up activities, supply and inventory coordination, third-party vendor coordination, patient recruitment and identification, and assisting with patient study visits.</p>\n<p>The ideal candidate will have a high school diploma or equivalent, knowledge of FDA regulations and ICH/GCP guidelines, and the ability to draw blood, run labs, and take vitals. Strong communication skills, teamwork, cooperation, self-awareness, and flexibility are also required.</p>\n<p>This role will be evaluated on patient experience, protocol management and adherence, and data quality. The successful candidate will lead with empathy for patients and care deeply about creating new access to clinical research in communities across the country.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_8c6d2818-9ca","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Topography","sameAs":"https://www.topography.com/","logo":"https://logos.yubhub.co/topography.com.png"},"x-apply-url":"https://jobs.lever.co/jointopo/57b71a88-3cd6-48ba-91f8-b64b070f9983","x-work-arrangement":"onsite","x-experience-level":"entry","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["FDA regulations","ICH/GCP guidelines","blood drawing","lab running","vital signs taking"],"x-skills-preferred":[],"datePosted":"2026-04-17T13:04:53.238Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Albuquerque"}},"employmentType":"FULL_TIME","occupationalCategory":"Research","industry":"Healthcare","skills":"FDA regulations, ICH/GCP guidelines, blood drawing, lab running, vital signs taking"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d67b1b38-d42"},"title":"Research Phlebotomist","description":"<p>Meet knownwell, a weight-inclusive healthcare company that is changing the way obesity care is delivered. We offer weight management, primary care, nutrition counseling, and health coaching. Our care model combines in-clinic and virtual care to bring support to patients where and when they need it.</p>\n<p>The Research Phlebotomist plays a vital hands-on role in the execution of clinical trials, serving as a key point of contact for study participants throughout their research journey. Working under the direction of the Clinical Research Coordinator and/or Clinical Research Manager, the Research Phlebotomist is primarily responsible for patient-facing activities, including study visits, specimen collection and processing, data entry, and clinical assessments.</p>\n<p><strong>Responsibilities</strong></p>\n<p>Patient Interaction &amp; Visit Support</p>\n<ul>\n<li>Serve as a primary point of contact for study participants during on-site visits, providing a welcoming and professional experience.</li>\n<li>Guide participants through study visit procedures, answering questions and ensuring they feel informed and comfortable throughout the process.</li>\n<li>Assist in the informed consent process, ensuring participants understand study expectations, risks, and benefits prior to enrollment.</li>\n<li>Monitor and document participant well-being during visits, escalating any safety concerns to the supervising Coordinator or Investigator promptly.</li>\n<li>Schedule and confirm participant appointments, sending reminders and managing visit logistics to support timely enrollment and retention.</li>\n</ul>\n<p>Clinical Assessments</p>\n<ul>\n<li>Perform and document vital signs, including blood pressure, heart rate, temperature, respiratory rate, and weight.</li>\n<li>Conduct electrocardiograms (EKGs) per protocol, ensuring proper lead placement and tracing quality.</li>\n<li>Perform phlebotomy (blood draws) in accordance with study protocols and applicable safety standards.</li>\n<li>Administer and document other protocol-specified assessments as trained and permitted by scope of practice.</li>\n</ul>\n<p>Specimen Collection &amp; Processing</p>\n<ul>\n<li>Collect, process, label, and store biological samples (blood, urine, etc.) per study protocol and applicable regulatory requirements.</li>\n<li>Ensure proper cold-chain handling and timely shipment of samples to central labs or sponsors.</li>\n<li>Maintain specimen logs and chain-of-custody documentation accurately.</li>\n<li>Ensure proper disposal of biohazardous materials in compliance with institutional and regulatory standards.</li>\n</ul>\n<p>Data Entry &amp; Documentation</p>\n<ul>\n<li>Accurately enter study data into the clinical trial management system (CTMS) and/or electronic data capture (EDC) systems in a timely manner.</li>\n<li>Complete and maintain source documentation for all participant visits, assessments, and clinical activities.</li>\n<li>Perform basic quality control checks on data entry to ensure accuracy and completeness.</li>\n<li>Flag discrepancies or missing data to the supervising Coordinator for resolution.</li>\n</ul>\n<p>Site &amp; 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