Lab Coordinator / Phlebotomist

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  "last_changed_at": "2026-06-06T20:05:25.710Z",
  "active_status": "deleted"
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{
  "language": "en",
  "location": {
    "raw": "Accel Research Sites - DeLand, FL, DeLand, FL",
    "city": "Accel Research Sites - DeLand",
    "region": "FL",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.9
  },
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  "inferred_at": "2026-06-05T01:28:27.170Z",
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    "language": "en",
    "location": {
      "raw": "Accel Research Sites - DeLand, FL, DeLand, FL",
      "city": "Accel Research Sites - DeLand",
      "region": "FL",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.9
    },
    "countries": [
      "United States"
    ]
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  "remote_policy": null,
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  "workplace_type": "on_site",
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{}

{
  "id": "466865",
  "job": {
    "id": "476495",
    "division": null,
    "department": {
      "id": "21118",
      "name": "Operations "
    },
    "requisition_id": "PIN-1448",
    "structure_custom_group_one": null
  },
  "url": "https://alcanzaclinical.pinpointhq.com/en/postings/1be63999-a8c0-4bb2-83e8-287f4232a030",
  "path": "/en/postings/1be63999-a8c0-4bb2-83e8-287f4232a030",
  "title": "Lab Coordinator / Phlebotomist",
  "benefits": "<ul><li><!--block-->Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.&nbsp;</li><li><!--block-->Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.</li></ul><div><!--block--><br></div>",
  "location": {
    "id": "19118",
    "city": "DeLand",
    "name": "Accel Research Sites - DeLand, FL",
    "province": "FL",
    "postal_code": "32720"
  },
  "deadline_at": null,
  "description": "<div><!--block-->Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. <br><br>The <strong>Lab Coordinator</strong> works to ensure the execution of assigned lab procedures in compliance with GCP, ICH, FED and HIPAA regulations, company SOPs, and policies. &nbsp;</div>",
  "compensation": null,
  "reporting_to": "Diana Toney",
  "workplace_type": "onsite",
  "benefits_header": "Benefits",
  "employment_type": "full_time",
  "workplace_type_text": "Onsite",
  "compensation_maximum": null,
  "compensation_minimum": null,
  "compensation_visible": false,
  "employment_type_text": "Full Time",
  "key_responsibilities": "<div><!--block--><strong>Essential Job Duties: </strong>Responsibilities may include but are not limited to:<br><br></div><ul><li><!--block-->Draw and process specimens according to each trial’s requirements</li><li><!--block-->Assist with specimen shipments to central labs and ensure proper shipping methods have been observed</li><li><!--block-->Monitor expiration dates on lab equipment and supplies&nbsp;</li><li><!--block-->Unpack and put away incoming lab supply shipments</li><li><!--block-->Monitor and maintain both general and study-specific lab inventory, and ensure study-specific lab supplies are ready for new study start-up</li><li><!--block-->Transport samples</li><li><!--block-->Provide mentoring to new hires and allow them to shadow you as they learn.</li><li><!--block-->Complete and renew CITI GCP and IATA training as required.</li><li><!--block-->Attend SIVs when needed, and complete all sponsor-required lab training.</li><li><!--block-->May support other clinical research-related activities such as recruitment, EDC and QA/Chart review as needed.</li><li><!--block-->Ensuring compliance with company SOPs, FDA/HIPAA regulations, ICF documentation, and GCP guidelines</li><li><!--block-->Maintaining confidentiality of patients, customers, and company information, and</li><li><!--block-->Performing other related activities as assigned.</li></ul>",
  "compensation_currency": null,
  "compensation_frequency": null,
  "skills_knowledge_expertise": "<div><!--block--><strong>Minimum Qualifications</strong>:&nbsp; High School diploma or equivalent and a minimum of 1 year of clinical laboratory processing experience is required. Associates degree is preferred.&nbsp; Bilingual (English/Spanish) skills are a plus. <br> <br> <strong>Required Skills:&nbsp;<br></strong><br></div><ul><li><!--block-->Proficiency with computer applications such as Microsoft applications, email, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).</li><li><!--block-->Strong organizational skills and attention to detail.</li><li><!--block-->Well-developed written and verbal communication skills.&nbsp;</li><li><!--block-->Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.</li><li><!--block-->Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.</li><li><!--block-->Must be professional, respectful of others, self-motivated, and have a strong work ethic.</li><li><!--block-->Must possess a high degree of integrity and dependability.</li><li><!--block-->Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.</li></ul>",
  "key_responsibilities_header": "Key Responsibilities",
  "skills_knowledge_expertise_header": "Skills, Knowledge and Expertise"
}