Visiting Clinical Research Coordinator - Department of Medicine, Division of Breathe Chicago Center

{
  "content_hash": "092bc10b6c8fba5a859cc41acf4778370f2c197cbb00b330d0f2c6fc39f0813d",
  "source_hash": "0f7b5cbcdc162a4c9d50fe2df8ba34cf466f38c84ca82d43380126346000d820",
  "last_changed_at": "2026-05-29T22:41:12.882Z",
  "active_status": "active"
}

{
  "language": "en",
  "location": {
    "raw": "Chicago, IL, US",
    "city": "Chicago",
    "region": "IL",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.98
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-06T10:03:50.045Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Chicago, IL, US",
      "city": "Chicago",
      "region": "IL",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.98
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": null,
  "salary_currency": null
}

{}

{
  "locations": [
    {
      "city": "Chicago",
      "state": "IL",
      "country": "US"
    }
  ],
  "requisitionId": 19965,
  "displayJobTitle": "Visiting Clinical Research Coordinator - Department of Medicine, Division of Breathe Chicago Center",
  "externalDescription": "Position Summary Clinical Research Coordinators support research activities across a range of sponsored studies (Federal, industry, foundation, etc.) as part of a cross-functional team that also includes Principal Investigators, physicians, nurses, project managers, as well as lab, data, and admin staff. Clinical Research Coordinators are responsible for the daily operations of one or more studies in the areas of protocol implementation and management, participant recruitment and retention, executing informed consent, and compliance with regulatory requirements. This role participates in recruitment, screening, scheduling, testing, and data management to achieve recruitment and visit completion targets and adhere to protocol requirements. Coordinators routinely monitor and report on study performance. Duties Responsibilities Duties and Responsibilities:_x000d_ _x000d_ Protocol Implementation and Management_x000d_ •\tConduct visits including anthropometric measurements and complex tests. Maintain detailed records of results. Enter data into the appropriate system as required per protocol and within required study timeline._x000d_ •\tCoordinate comprehensive patient protocol treatment schedules to maintain compliance to protocol requirements. _x000d_ •\tLead workstream, project, and/or test as identified by supervisor. _x000d_ •\tAssist in data cleaning as assigned. _x000d_ Participant Recruitment and Retention_x000d_ •\tContribute to the development of, and implement, strategies for optimizing the recruitment of research participants. Assist physicians and clinical staff in the identification of prospective participants._x000d_ •\tAssist with outreach to and liaison with staff at community events, contribute to presentations aimed at participant recruitment._x000d_ •\tScreen participants for relevant and applicable studies. _x000d_ •\tSchedule participant visits. _x000d_ •\tAssist with participant engagement activities such as preparing materials, ensuring timely payments, and guiding participants around campus. _x000d_ •\tAnalyze retention rates and contribute to retention plans._x000d_ Informed Consent and Regulatory Compliance_x000d_ •\tExecute informed consent process and monitor participant status; Enroll participants into programs, explaining the research protocols to the clients and supporting family/friends, and obtain appropriate consent forms. _x000d_ •\tEnsure that participant enrollment and research activities comply with established protocols._x000d_ •\tMaintain detailed records of results and prepare written reports, including vitals and measurements, and document and convey adverse events._x000d_ •\tIdentify adverse events and protocol deviations and assist with reporting._x000d_ Other related duties_x000d_ •\tAssist investigators in preparing study data, literature reviews, analysis for meeting presentations and publications. _x000d_ •\tDevelop and conduct internal presentations._x000d_ •\tParticipate in special projects as assigned._x000d_ Perform other related duties and participate in special projects as assigned. ",
  "postingEffectiveDate": "5/29/2026",
  "postingExpirationDate": "6/20/2026"
}