Clinical Research Coordinator

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  "last_changed_at": "2026-05-31T17:45:56.288Z",
  "active_status": "active"
}

{
  "language": "en",
  "location": {
    "raw": "Tampa Bay Medical Research - Clearwater, Clearwater, Florida",
    "city": "Clearwater",
    "region": "FL",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
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  "inferred_at": "2026-06-06T20:05:25.707Z",
  "launch_scope": {
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    "included": true,
    "language": "en",
    "location": {
      "raw": "Tampa Bay Medical Research - Clearwater, Clearwater, Florida",
      "city": "Clearwater",
      "region": "FL",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
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  "remote_policy": null,
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  "workplace_type": "on_site",
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{}

{
  "id": "513567",
  "job": {
    "id": "520063",
    "division": null,
    "department": {
      "id": "21118",
      "name": "Operations "
    },
    "requisition_id": "PIN-1614",
    "structure_custom_group_one": null
  },
  "url": "https://alcanzaclinical.pinpointhq.com/en/postings/ac578255-b1ed-4e7b-aecf-e7a0b251c96b",
  "path": "/en/postings/ac578255-b1ed-4e7b-aecf-e7a0b251c96b",
  "title": "Clinical Research Coordinator ",
  "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>",
  "location": {
    "id": "77963",
    "city": "Clearwater",
    "name": "Tampa Bay Medical Research - Clearwater",
    "province": "Florida",
    "postal_code": "33761"
  },
  "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>Clinical Research Coordinator (CRC)</strong> works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. &nbsp;</div>",
  "compensation": null,
  "reporting_to": "Brie jackson ",
  "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>In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:</div><ul><li><!--block-->Screening of patients for study enrollment;&nbsp;</li><li><!--block-->Patient consents;</li><li><!--block-->Patient follow-up visits;</li><li><!--block-->Documenting in source clinic charts;</li><li><!--block-->Entering data in EDC and answers queries;</li><li><!--block-->Obtaining vital signs and ECGs;</li><li><!--block-->May perform basic lab procedures per protocol, such as:&nbsp; blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;&nbsp;</li><li><!--block-->Requesting and tracking medical record requests;</li><li><!--block-->Updating and maintaining logs, chart filings;&nbsp;</li><li><!--block-->Maintaining &amp; ordering study specific supplies;]</li><li><!--block-->Scheduling subjects for study visits and conducts appointment reminders;</li><li><!--block-->Building/updating source as needed;</li><li><!--block-->Conducting monitoring visits and resolves issues as needed in a timely manner;</li><li><!--block-->Ensuring study related reports and patient results are reviewed by investigator in a timely manner;</li><li><!--block-->Filing SAE/Deviation reports to Sponsor and IRB as needed;</li><li><!--block-->Documenting and reporting adverse events;</li><li><!--block-->Reporting non-compliance to appropriate staff in timely manner;</li><li><!--block-->Maintaining positive and effective communication with clients and team members;</li><li><!--block-->Always practicing ALCOAC principles with all documentation;</li><li><!--block-->May assist with study recruitment, patient enrollment, and tracking as needed;</li><li><!--block-->Maintaining confidentiality of patients, customers and company information, and;</li><li><!--block-->Performing all other duties as requested or assigned.</li><li><!--block-->Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;</li><li><!--block-->Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;</li><li><!--block-->May set up, train and maintain all technology needed for studies.</li></ul>",
  "compensation_currency": null,
  "compensation_frequency": null,
  "skills_knowledge_expertise": "<div><!--block--><strong>Minimum Qualifications</strong>:&nbsp; A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required.&nbsp; Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred.&nbsp; Bi-lingual (English / Spanish) proficiency is a plus. <br> <strong><br>&nbsp;Required Skills:&nbsp;</strong></div><ul><li><!--block-->Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);</li><li><!--block-->Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc</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 work under minimal supervision, identify problems and implement solutions.</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"
}