Clinical Project Manager (US)

{
  "content_hash": "8ad8f6b2b9e84eba69f0ed8e2a332cbe8dc6d3b580ee15cb60592220e89f67a6",
  "source_hash": "0b04035e3767e28e834f565c19a1519d1c4710de1cb1fd24aad4365d68682026",
  "last_changed_at": "2026-05-29T07:01:33.822Z",
  "active_status": "active"
}

{
  "language": "en",
  "location": {
    "raw": "Raleigh-Durham, North Carolina",
    "city": "Raleigh-Durham",
    "region": "NC",
    "country": "United States",
    "is_remote": true,
    "confidence": 0.85
  },
  "salary_max": 159000,
  "salary_min": 95500,
  "inferred_at": "2026-06-06T07:57:11.639Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Raleigh-Durham, North Carolina",
      "city": "Raleigh-Durham",
      "region": "NC",
      "country": "United States",
      "is_remote": true,
      "confidence": 0.85
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": "remote",
  "salary_period": "year",
  "workplace_type": "remote",
  "salary_currency": "USD"
}

{}

{
  "lists": [
    {
      "text": "Project Management ",
      "content": "\n<li>Manage the planning, execution, progress and completion of assigned clinical research projects.</li>\n<li>Work with functional experts to ensure all project activities comply with applicable regulations, guidelines, and corporate policies.</li>\n<li>Maintain operational, financial and regulatory integrity and safety.</li>\n<li>Develop and/or participate in the development of project communications, training, regulatory submissions and/or audits and selection of third party vendors as required.</li>\n\n<div>&nbsp;</div>"
    },
    {
      "text": "Documents and Tools",
      "content": "\n<li>Manage a cross-functional team to ensure the appropriate creation, delivery, maintenance and disposal of all related data, documents, equipment and tools, including protocols, SOPs, informed consent forms, case report forms and instructions.</li>\n<li>Prepare investigator updates and other project related reports as required to support the proper conduct and execution throughout the life cycle of assigned projects.</li>\n"
    },
    {
      "text": "Project Team Performance ",
      "content": "\n<li>Identify, assign and monitor the completion of interdisciplinary project tasks that include site monitoring, CRF and database development and revision, data collection, patient safety/adverse event management, document management, statistical analysis and/or final report writing and publications.</li>\n<li>Ensure task completion performance meets or exceeds quality standards and sponsor/client, project and regulatory expectations and guidelines.</li>\n"
    },
    {
      "text": "Client/Sponsor Support ",
      "content": "\n<li>Act as primary liaison throughout the project life cycle ensuring client/sponsor expectations are appropriately managed by addressing and resolving queries/issues, planning and executing all project meetings, assisting with site and patient recruitment strategies and materials, assisting with the development of stakeholder training and by regularly providing sponsor/client with project status and update reports.</li>\n"
    },
    {
      "text": "Qualifications ",
      "content": "\n<li>Applicants should have a minimum of a Bachelor's Degree in a relevant field of study (Health Sciences, Clinical Research preferred) and 1-3 years of experience in clinical study management</li>\n<li>The successful candidate must exhibit the following skills: self-motivation with strong communication skills and a commitment to achieving positive results.</li>\n<li>Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results.</li>\n<li>Ability to engage in continuous learning and self-development.</li>\n<li>Ability to continually foster teamwork.&nbsp;</li>\n<li>Fluent in reading, writing, and speaking of English</li>\n"
    },
    {
      "text": "Working Conditions ",
      "content": "\n<li>Home Based</li>\n<li>Occasional travel</li>\n\n<div>&nbsp;</div>"
    }
  ],
  "country": "US",
  "createdAt": 1771942381699,
  "updatedAt": null,
  "categories": {
    "team": "Clinical Study Delivery - Clinical Study Management - Project Management",
    "location": "Raleigh-Durham, North Carolina",
    "commitment": "Full-time, Permanent",
    "department": "Clinical Services",
    "allLocations": [
      "Raleigh-Durham, North Carolina"
    ]
  },
  "salaryRange": {
    "max": 159000,
    "min": 95500,
    "currency": "USD",
    "interval": "per-year-salary"
  },
  "workplaceType": "remote"
}