Clinical Research Assistant / Medical Assistant

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

{
  "language": "en",
  "location": {
    "raw": "Tampa Bay Medical Research - Largo, Largo, Florida",
    "city": "Largo",
    "region": "FL",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": 0,
  "salary_min": 0,
  "inferred_at": "2026-06-06T20:05:25.707Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Tampa Bay Medical Research - Largo, Largo, Florida",
      "city": "Largo",
      "region": "FL",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": "on_site",
  "salary_currency": null
}

{}

{
  "id": "513815",
  "job": {
    "id": "493518",
    "division": null,
    "department": {
      "id": "21118",
      "name": "Operations "
    },
    "requisition_id": "PIN-1514",
    "structure_custom_group_one": null
  },
  "url": "https://alcanzaclinical.pinpointhq.com/en/postings/3c5d2c6d-2580-4bb7-8418-2f8f0e143ada",
  "path": "/en/postings/3c5d2c6d-2580-4bb7-8418-2f8f0e143ada",
  "title": "Clinical Research Assistant / Medical Assistant",
  "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": "77962",
    "city": "Largo",
    "name": "Tampa Bay Medical Research - Largo",
    "province": "Florida",
    "postal_code": "33777"
  },
  "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>Research Assistant (RA) </strong>provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.&nbsp; The RA performs clinical, lab, and administrative tasks as needed for the successful operation of the clinical research site.</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, assists with the execution of assigned studies, and support functions as needed. Responsibilities may include but are not limited to:&nbsp;</div><ul><li><!--block-->Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol:&nbsp;<ul><li><!--block-->Assists with the basic screening of patients for study enrollment;&nbsp;</li><li><!--block-->Assists with patient follow-up visits;&nbsp;</li><li><!--block-->Documents in source clinic charts;&nbsp;</li><li><!--block-->Enters data in EDC and answers queries;&nbsp;</li><li><!--block-->Obtains vital signs and ECGs;</li><li><!--block-->May perform blood draws;</li><li><!--block-->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-->Request and track medical record requests;&nbsp;</li><li><!--block-->Enters data in EDC and answers queries;&nbsp;</li><li><!--block-->Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and&nbsp;</li><li><!--block-->Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed;&nbsp;</li></ul></li><li><!--block-->Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.&nbsp; &nbsp;</li><li><!--block-->Assists the CRC and/or Manager with study recruitment, patient enrollment, and tracking as needed;&nbsp;</li><li><!--block-->Maintains strict confidentiality of patients, employees, customers and company information at all times and adheres to HIPAA Guidelines; and&nbsp;</li><li><!--block-->Perform all other duties as requested or assigned.&nbsp;</li></ul>",
  "compensation_currency": null,
  "compensation_frequency": null,
  "skills_knowledge_expertise": "<div><!--block--><strong>Minimum Qualifications</strong>: A High School diploma and 1 year of administrative / clinical experience is required. &nbsp; 1 year or more years of clinical research or clinical experience is preferred.&nbsp; Bi-lingual (English / Spanish) proficiency is a plus.</div><div><!--block--><br></div><div><!--block--><strong>Required Skills:</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-->Must possess strong organizational skills and attention to detail.</li><li><!--block-->Well-developed written and verbal communication skills.</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"
}