Clinical Research Physician (part time) - Metabolic: Endocrine, Hepatology, GI

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  "last_changed_at": "2026-05-31T17:45:56.288Z",
  "active_status": "active"
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{
  "language": "en",
  "location": {
    "raw": "Charleston, SC, North Charleston, South Carolina",
    "city": "Charleston",
    "region": "SC",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.9
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  "inferred_at": "2026-06-06T20:05:25.698Z",
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    "language": "en",
    "location": {
      "raw": "Charleston, SC, North Charleston, South Carolina",
      "city": "Charleston",
      "region": "SC",
      "country": "United States",
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      "confidence": 0.9
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    "countries": [
      "United States"
    ]
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  "remote_policy": null,
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  "workplace_type": "on_site",
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{}

{
  "id": "470354",
  "job": {
    "id": "480241",
    "division": null,
    "department": {
      "id": "21118",
      "name": "Operations "
    },
    "requisition_id": "PIN-1454",
    "structure_custom_group_one": null
  },
  "url": "https://alcanzaclinical.pinpointhq.com/en/postings/d76753e6-2832-435b-9475-7930dff7eb43",
  "path": "/en/postings/d76753e6-2832-435b-9475-7930dff7eb43",
  "title": "Clinical Research Physician (part time) - Metabolic: Endocrine, Hepatology, GI",
  "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": "11667",
    "city": "North Charleston",
    "name": "Coastal Carolina Research Center | Charleston, SC",
    "province": "South Carolina",
    "postal_code": "29405"
  },
  "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>Principal Investigator </strong>conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.</div>",
  "compensation": null,
  "reporting_to": "Mary Love",
  "workplace_type": "onsite",
  "benefits_header": "Benefits",
  "employment_type": "part_time",
  "workplace_type_text": "Onsite",
  "compensation_maximum": null,
  "compensation_minimum": null,
  "compensation_visible": false,
  "employment_type_text": "Part Time",
  "key_responsibilities": "<div><!--block--><strong>Essential Job Duties:</strong></div><ul><li><!--block-->Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs &amp; HIPAA guidelines, study protocols, as well as company policies and processes&nbsp;</li><li><!--block-->Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance</li><li><!--block-->Evaluates and assesses participants to ensure only eligible participants enroll into the trials.</li><li><!--block-->Participates and engages in successful delivery and retention of study participants.</li><li><!--block-->Interacts positively and collaboratively with sponsors, clients and team members.</li><li><!--block-->Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.</li><li><!--block-->Actively involved in protocol training for staff.</li><li><!--block-->Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.</li><li><!--block-->Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.</li></ul><div><!--block--><br></div>",
  "compensation_currency": null,
  "compensation_frequency": null,
  "skills_knowledge_expertise": "<div><!--block--><strong>Minimum Qualifications:</strong>&nbsp; MD or DO degree, an active physician license (in good standing) in the state of practice for this role is required.&nbsp; Experience in clinical research preferred. Board certification in area of specialty is required. CPR required / ACLS preferred.<br><br></div><div><!--block--><strong>Required Skills:&nbsp;</strong></div><ul><li><!--block-->Clinical skills and clinical procedures based in area of specialty.&nbsp;</li><li><!--block-->Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).&nbsp;</li><li><!--block-->Must possess strong organizational skills, attention to detail, and math proficiency.</li><li><!--block-->Well-developed written and verbal communication skills.&nbsp; Bi-lingual (English / Spanish) proficiency is highly preferred.</li><li><!--block-->Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers. &nbsp;</li><li><!--block-->Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.</li><li><!--block-->Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.</li><li><!--block-->Must possess a high degree of urgency, self-motivation, integrity and dependability.</li><li><!--block-->Ability to work independently to identify problems and implement solutions.&nbsp;</li><li><!--block-->Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.</li></ul><div><!--block--><br></div>",
  "key_responsibilities_header": "Key Responsibilities",
  "skills_knowledge_expertise_header": "Skills, Knowledge and Expertise"
}