Prinicipal Investigator

{
  "content_hash": "b078a5bd3619c690606d640a16131dc9e8ee94cc9f8430919e2c0fc017acfcad",
  "source_hash": "7f4571e3372cc19bce228d23c8c237215f6b1b3783991aad5c5ce5add4662559",
  "last_changed_at": "2026-05-30T06:04:30.139Z",
  "active_status": "active"
}

{
  "language": "en",
  "location": {
    "raw": "Covington Clinic",
    "city": "Covington",
    "region": "LA",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-06T13:34:11.393Z",
  "launch_scope": {
    "reason": "paylocity_production_catalog",
    "included": true,
    "location": {
      "raw": "Covington Clinic",
      "city": "Covington",
      "region": "LA",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": null,
  "salary_currency": null
}

{}

{
  "detail": {
    "url": "https://recruiting.paylocity.com/recruiting/jobs/Details/3913227/Prolerity-Clinical-Research/Prinicipal-Investigator",
    "job_type": null,
    "pageData": {
      "jobTitle": "Prinicipal Investigator",
      "moduleName": "Prolerity Clinical Research",
      "showSocialWidget": true
    },
    "apply_path": "/Recruiting/jobs/Apply/3913227",
    "html_title": "Prolerity Clinical Research - Prinicipal Investigator",
    "description_html": "<p><strong>Position Summary</strong></p><p>The Principal Investigator (PI) provides medical leadership and regulatory oversight for industry-sponsored clinical trials conducted at the site. The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA regulations and ICH-GCP guidelines, while working within a highly supported research model that includes full-time, experienced mid-level Sub-Investigators (NPs/PAs) and dedicated clinical research staff.</p><p><br></p><p>This role is well-suited for both experienced PIs and clinicians new to the PI role, offering robust operational support that allows the PI to focus on medical decision-making, subject safety, regulatory compliance, and Sponsor collaboration.</p><p>________________________________________</p><p><strong>Key Responsibilities</strong></p><p><strong>Clinical &amp; Regulatory Oversight</strong></p><ul><li>Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic areas</li><li>Maintain ultimate regulatory responsibility for study conduct, subject safety, and protocol compliance</li><li>Appropriately delegate study-related activities to qualified Sub-Investigators and research staff while providing ongoing supervision in accordance with FDA regulations and ICH-GCP</li><li>Provide medical oversight for subject eligibility, treatment decisions, and clinical assessments</li><li>Review, assess, and approve adverse events (AEs), serious adverse events (SAEs), safety narratives, and protocol deviations</li><li>Ensure informed consent processes are conducted appropriately and consistently</li><li>Participate in monitoring visits, audits, and regulatory inspections as required</li></ul><p><strong>Collaborative Research Model</strong></p><ul><li>Supervise and collaborate with full-time mid-level Sub-Investigators (NPs/PAs) who support protocol-required visits and assessments under the PI’s oversight</li><li>Work closely with Study Coordinators and site leadership to ensure high-quality study execution</li><li>Contribute to a culture of quality, compliance, and patient-centered research</li></ul><p><strong>Patient Engagement &amp; Community Collaboration</strong></p><ul><li>Support patient engagement and retention initiatives designed to improve awareness of clinical research opportunities</li><li>Collaborate with local healthcare providers, referral partners, and community organizations to provide education and information about ongoing and upcoming research studies</li><li>Serve as a clinical resource to help expand access to research for the local patient population</li></ul><p><strong>Sponsor Engagement &amp; Business Development</strong></p><ul><li>Serve as a medical and scientific representative of the site in interactions with Sponsors and CROs</li><li>Participate in feasibility assessments, protocol review, and protocol design consultation when requested</li><li>Support business development efforts through key client meetings, bid defenses, and therapeutic area discussions</li><li>Contribute clinical insight to support study selection and research program growth</li></ul><p><br></p>",
    "jsonld_jobposting": {
      "@type": "JobPosting",
      "title": "Prinicipal Investigator",
      "@context": "https://schema.org",
      "datePosted": "2026-03-06T17:43:03-06:00",
      "description": "<p>Description</p><p><strong>Position Summary</strong></p><p>The Principal Investigator (PI) provides medical leadership and regulatory oversight for industry-sponsored clinical trials conducted at the site. The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA regulations and ICH-GCP guidelines, while working within a highly supported research model that includes full-time, experienced mid-level Sub-Investigators (NPs/PAs) and dedicated clinical research staff.</p><p><br/></p><p>This role is well-suited for both experienced PIs and clinicians new to the PI role, offering robust operational support that allows the PI to focus on medical decision-making, subject safety, regulatory compliance, and Sponsor collaboration.</p><p>________________________________________</p><p><strong>Key Responsibilities</strong></p><p><strong>Clinical & Regulatory Oversight</strong></p><ul><li>Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic areas</li><li>Maintain ultimate regulatory responsibility for study conduct, subject safety, and protocol compliance</li><li>Appropriately delegate study-related activities to qualified Sub-Investigators and research staff while providing ongoing supervision in accordance with FDA regulations and ICH-GCP</li><li>Provide medical oversight for subject eligibility, treatment decisions, and clinical assessments</li><li>Review, assess, and approve adverse events (AEs), serious adverse events (SAEs), safety narratives, and protocol deviations</li><li>Ensure informed consent processes are conducted appropriately and consistently</li><li>Participate in monitoring visits, audits, and regulatory inspections as required</li></ul><p><strong>Collaborative Research Model</strong></p><ul><li>Supervise and collaborate with full-time mid-level Sub-Investigators (NPs/PAs) who support protocol-required visits and assessments under the PI’s oversight</li><li>Work closely with Study Coordinators and site leadership to ensure high-quality study execution</li><li>Contribute to a culture of quality, compliance, and patient-centered research</li></ul><p><strong>Patient Engagement & Community Collaboration</strong></p><ul><li>Support patient engagement and retention initiatives designed to improve awareness of clinical research opportunities</li><li>Collaborate with local healthcare providers, referral partners, and community organizations to provide education and information about ongoing and upcoming research studies</li><li>Serve as a clinical resource to help expand access to research for the local patient population</li></ul><p><strong>Sponsor Engagement & Business Development</strong></p><ul><li>Serve as a medical and scientific representative of the site in interactions with Sponsors and CROs</li><li>Participate in feasibility assessments, protocol review, and protocol design consultation when requested</li><li>Support business development efforts through key client meetings, bid defenses, and therapeutic area discussions</li><li>Contribute clinical insight to support study selection and research program growth</li></ul><p><br/></p><p>Requirements</p><p><strong>Specialty Focus</strong></p><p><strong>Psychiatry</strong></p><ul><li>Mood disorders, anxiety disorders, depression, schizophrenia, and related psychiatric indications</li></ul><p><strong>CNS</strong></p><ul><li>Alzheimer’s disease, Parkinson’s disease, neurodegenerative, cognitive, and neurological disorders</li></ul><p><strong>Gastroenterology</strong></p><ul><li>NASH/MASH, IBS-C, IBS-D, metabolic liver disease, and functional GI disorders</li></ul><p><br/></p><p><strong>Qualifications</strong></p><ul><li>MD or DO (required)</li><li>Board-certified or board-eligible in relevant specialty</li><li>Active, unrestricted medical license</li><li>Interest in or prior experience with industry-sponsored clinical research</li><li>Strong understanding of, or willingness to be trained in, FDA regulations and ICH-GCP</li><li>Excellent communication, documentation, and collaborative leadership skills</li></ul><p><br/></p>",
      "jobLocation": {
        "@type": "Place",
        "address": {
          "@type": "PostalAddress",
          "postalCode": "70433",
          "addressRegion": "LA",
          "streetAddress": "1970 N Highway 190",
          "addressCountry": "US",
          "addressLocality": "Covington"
        }
      },
      "hiringOrganization": {
        "logo": "https://recruiting.paylocity.com/recruiting/jobs/GetLogoFile?moduleId=33974",
        "name": "Tandem Intermediate LLC",
        "@type": "Organization"
      }
    },
    "requirements_html": "<p><strong>Specialty Focus</strong></p><p><strong>Psychiatry</strong></p><ul><li>Mood disorders, anxiety disorders, depression, schizophrenia, and related psychiatric indications</li></ul><p><strong>CNS</strong></p><ul><li>Alzheimer’s disease, Parkinson’s disease, neurodegenerative, cognitive, and neurological disorders</li></ul><p><strong>Gastroenterology</strong></p><ul><li>NASH/MASH, IBS-C, IBS-D, metabolic liver disease, and functional GI disorders</li></ul><p><br></p><p><strong>Qualifications</strong></p><ul><li>MD or DO (required)</li><li>Board-certified or board-eligible in relevant specialty</li><li>Active, unrestricted medical license</li><li>Interest in or prior experience with industry-sponsored clinical research</li><li>Strong understanding of, or willingness to be trained in, FDA regulations and ICH-GCP</li><li>Excellent communication, documentation, and collaborative leadership skills</li></ul><p><br></p>",
    "requirements_text": "Specialty Focus\n Psychiatry\n Mood disorders, anxiety disorders, depression, schizophrenia, and related psychiatric indications\n CNS\n Alzheimer’s disease, Parkinson’s disease, neurodegenerative, cognitive, and neurological disorders\n Gastroenterology\n NASH/MASH, IBS-C, IBS-D, metabolic liver disease, and functional GI disorders\n Qualifications\n MD or DO (required)\n Board-certified or board-eligible in relevant specialty\n Active, unrestricted medical license\n Interest in or prior experience with industry-sponsored clinical research\n Strong understanding of, or willingness to be trained in, FDA regulations and ICH-GCP\n Excellent communication, documentation, and collaborative leadership skills"
  },
  "list_job": {
    "JobId": 3913227,
    "IsRemote": false,
    "JobTitle": "Prinicipal Investigator",
    "IsInternal": false,
    "Description": "",
    "JobLocation": {
      "Zip": "70433",
      "City": "Covington",
      "Name": "Covington Clinic",
      "Metro": null,
      "State": "LA",
      "County": "St. Tammany Parish",
      "Address": "1970 N Highway 190",
      "Country": "USA",
      "Address2": "Suite C",
      "ModuleId": 33974,
      "LocationId": 3838084,
      "SmartyAddressId": "00000000-0000-0000-0000-000000000000"
    },
    "LocationName": "Covington Clinic",
    "PublishedDate": "2026-03-06T11:43:03-06:00",
    "HiringDepartment": null,
    "IndeedRemoteType": 2,
    "ShouldDisplayLocation": true
  },
  "detail_errors": []
}