Clinical Research Nurse

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    "html_title": "Prolerity Clinical Research - Clinical Research Nurse",
    "description_html": "<p>The Clinical Research Nurse oversees the daily activities of clinical research studies. They</p><p>work closely with the clinical teams and investigators to ensure that all required</p><p>procedures and visits occur according to protocol specific guidelines.</p><p><strong>RESPONSIBILITIES</strong></p><ul><li>&nbsp;Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator</li><li>&nbsp;Adhere strictly to the study protocol; obtain exemptions when necessary/appropriate</li><li>&nbsp;Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator</li><li>&nbsp;Articulate all pertinent issues to the PI or document by email/letter or during meetings</li><li>&nbsp;Collect initial psychiatric and medical information by interviewing patients and by accessing other appropriate sources</li><li>&nbsp;Ensure a flow of communication including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitor(s), Auditors and any marketing groups hired by the Sponsor</li><li>&nbsp;Utilize various rating scales and maintain interrater reliability with other clinicians</li><li>&nbsp;Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, specimen packaging</li><li>&nbsp;Maintain timely source documentation as well as sponsor required information.</li><li>&nbsp;Dispense and maintain accurate records of study medication</li><li>&nbsp;Educate patients and family regarding their particular study and clinical drug trials in general.</li><li>&nbsp;Complete all monitor and sponsor queries in a timely manner</li><li>&nbsp;Provide appropriate community resource referrals to patients, caretakers, and family at conclusion of patient’s participation in study</li></ul>",
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      "datePosted": "2026-05-21T15:32:46-05:00",
      "description": "<p>Description</p><p>The Clinical Research Nurse oversees the daily activities of clinical research studies. They</p><p>work closely with the clinical teams and investigators to ensure that all required</p><p>procedures and visits occur according to protocol specific guidelines.</p><p><strong>RESPONSIBILITIES</strong></p><ul><li> Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator</li><li> Adhere strictly to the study protocol; obtain exemptions when necessary/appropriate</li><li> Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator</li><li> Articulate all pertinent issues to the PI or document by email/letter or during meetings</li><li> Collect initial psychiatric and medical information by interviewing patients and by accessing other appropriate sources</li><li> Ensure a flow of communication including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitor(s), Auditors and any marketing groups hired by the Sponsor</li><li> Utilize various rating scales and maintain interrater reliability with other clinicians</li><li> Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, specimen packaging</li><li> Maintain timely source documentation as well as sponsor required information.</li><li> Dispense and maintain accurate records of study medication</li><li> Educate patients and family regarding their particular study and clinical drug trials in general.</li><li> Complete all monitor and sponsor queries in a timely manner</li><li> Provide appropriate community resource referrals to patients, caretakers, and family at conclusion of patient’s participation in study</li></ul><p>Requirements</p><ul><li>Ability to communicate clearly and effectively (written and verbal)</li><li> Ability to communicate in an active multi-office environment</li><li> Must possess excellent interpersonal and customer service skills</li><li> Ability to multi-task, organize, prioritize appropriately, and work well both individually and as part of a team</li><li> Ability to use time productively and contribute to high levels of company operational efficiency and effectiveness</li><li> Ability to maintain confidentiality of information</li><li> Ability to efficiently operate all job-related office equipment (telephone, computer, calculator, fax, copier, study-specific equipment)</li></ul><p><strong>Required Experience</strong></p><ul><li> Bachelor’s degree required</li><li> RN licensure</li><li> Experience as a Clinical Research Coordinator (CRC) or Research Assistant</li></ul>",
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    "requirements_html": "<ul><li>Ability to communicate clearly and effectively (written and verbal)</li><li>&nbsp;Ability to communicate in an active multi-office environment</li><li>&nbsp;Must possess excellent interpersonal and customer service skills</li><li>&nbsp;Ability to multi-task, organize, prioritize appropriately, and work well both individually and as part of a team</li><li>&nbsp;Ability to use time productively and contribute to high levels of company operational efficiency and effectiveness</li><li>&nbsp;Ability to maintain confidentiality of information</li><li>&nbsp;Ability to efficiently operate all job-related office equipment (telephone, computer, calculator, fax, copier, study-specific equipment)</li></ul><p><strong>Required Experience</strong></p><ul><li>&nbsp;Bachelor’s degree required</li><li>&nbsp;RN licensure</li><li>&nbsp;Experience as a Clinical Research Coordinator (CRC) or Research Assistant</li></ul>",
    "requirements_text": "Ability to communicate clearly and effectively (written and verbal)\n Ability to communicate in an active multi-office environment\n Must possess excellent interpersonal and customer service skills\n Ability to multi-task, organize, prioritize appropriately, and work well both individually and as part of a team\n Ability to use time productively and contribute to high levels of company operational efficiency and effectiveness\n Ability to maintain confidentiality of information\n Ability to efficiently operate all job-related office equipment (telephone, computer, calculator, fax, copier, study-specific equipment)\n Required Experience\n Bachelor’s degree required\n RN licensure\n Experience as a Clinical Research Coordinator (CRC) or Research Assistant"
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