{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/title/research-phlebotomist"},"x-facet":{"type":"title","slug":"research-phlebotomist","display":"Research Phlebotomist","count":1},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@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; Operational Support</p>\n<ul>\n<li>Assist in preparing exam rooms and ensuring all equipment and supplies are ready prior to study visits.</li>\n<li>Support the Coordinator with site initiation, monitoring visits, and closeout activities as directed.</li>\n<li>Maintain adequate inventory of study supplies and assist with the receipt and storage of study materials.</li>\n<li>Support study staff training on visit procedures as needed.</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>High school diploma or GED required; associate or bachelor’s degree in a health-related field preferred.</li>\n<li>Medical Assistant (MA) certification, or equivalent clinical training/experience.</li>\n<li>GCP certification required (or willingness to obtain within 90 days of hire).</li>\n<li>1+ years of experience as a Medical Assistant or in a clinical setting required.</li>\n<li>Prior clinical research experience is preferred but not required, training will be provided.</li>\n<li>Experience in performing phlebotomy, EKGs, and vital signs in a clinical environment required.</li>\n</ul>\n<p><strong>Preferred Qualifications</strong></p>\n<ul>\n<li>Strong phlebotomy skills required.</li>\n<li>Proficiency in EKG administration and basic clinical assessments.</li>\n<li>Excellent interpersonal and communication skills; ability to build rapport with diverse patient populations.</li>\n<li>Strong attention to detail and commitment to accurate documentation.</li>\n<li>Ability to manage multiple tasks and prioritize effectively in a fast-paced environment.</li>\n<li>Comfortable working both independently and as part of a multidisciplinary team.</li>\n<li>Basic proficiency with electronic health records (EHR) and/or data entry systems.</li>\n</ul>\n<p><strong>Additional Information</strong></p>\n<ul>\n<li>On-site Opportunity</li>\n<li>Medical, dental, and vision insurance</li>\n<li>401K retirement plan with company match</li>\n<li>Up to 20 days of PTO per year + company holidays</li>\n<li>Up to 14 weeks of parental leave (12 for non-birthing parents)</li>\n</ul>\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_d67b1b38-d42","directApply":true,"hiringOrganization":{"@type":"Organization","name":"knownwell, Inc.","sameAs":"https://www.knownwell.com/","logo":"https://logos.yubhub.co/knownwell.com.png"},"x-apply-url":"https://jobs.lever.co/knownwell/e7f83923-2aba-40fc-a0af-85de15880598","x-work-arrangement":"hybrid","x-experience-level":"entry","x-job-type":"full-time","x-salary-range":"$45,000-60,000 per year","x-skills-required":["phlebotomy","EKG administration","vital signs","data entry","clinical trials","GCP certification"],"x-skills-preferred":["electronic health records","data entry systems","communication skills","interpersonal skills"],"datePosted":"2026-04-17T12:40:23.863Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Needham"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"phlebotomy, EKG administration, vital signs, data entry, clinical trials, GCP certification, electronic health records, data entry systems, communication skills, interpersonal skills","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":45000,"maxValue":60000,"unitText":"YEAR"}}}]}