Clinical Research Nurse

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  "last_changed_at": "2026-06-06T09:44:42.579Z",
  "active_status": "active"
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  "location": {
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    "title": "Clinical Research Nurse",
    "postedOn": "Posted Yesterday",
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    "id": "c13f5ade4bf11000bcd48c94f4170000",
    "title": "Clinical Research Nurse",
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    "jobReqId": "R0000041741",
    "location": "Germany - Berlin",
    "postedOn": "Posted Yesterday",
    "timeType": "Full time",
    "logoImage": {
      "alt": "Parexel",
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    "startDate": "2026-06-05",
    "externalUrl": "https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/Germany---Berlin/Clinical-Research-Nurse_R0000041741-1",
    "jobPostingId": "Clinical-Research-Nurse_R0000041741-1",
    "jobDescription": "<p><b>When our values align, there&#39;s no limit to what we can achieve.</b><br /> <br />At Parexel, we all share the same goal - to improve the world&#39;s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.</p><p>Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we&#39;re committed to making a difference.</p><p></p><p></p><p>We are seeking a dedicated Clinical Research Nurse to join our Clinical Pharmacology Research Unit (CPRU). <br />In this role, you will provide comprehensive clinical nursing care to study participants while ensuring strict adherence to departmental policies, established nursing standards, and ICH/GCP guidelines. You will be instrumental in delivering high-quality clinical research support across multiple concurrent studies.</p><p></p><p><b>Key Responsibilities:</b><br /><u>Study Coordination &amp; Support</u><br />-    Coordinate and provide continuity of support across allocated studies in collaboration with the Clinical Research Coordinator<br />-    Support all study activities, documentation processes, and special requirements<br />-    Ensure subject safety and accurate medical data documentation in accordance with case report forms (CRFs), study protocols, and ICH/GCP guidelines<br />Study Preparation &amp; Organization<br />-    Verify and maintain informed consent documentation for all study volunteers<br />-    Organize and maintain study-specific materials and medical devices<br />-    Prepare and maintain clinical equipment and safe study environments<br />-    Configure ward areas to meet study-specific requirements<br />-    Provide comprehensive care and support to volunteers from admission through discharge<br /><u>Subject Assessments &amp; Investigations</u><br />-    Perform physiological measurements including ECG, blood pressure, lung function testing, and venipuncture according to study protocol<br />-    Document all investigations accurately and completely<br />-    Prepare and instruct subjects for neuro-physiologic measurements as required<br />-    Perform EEG registrations and polysomnographic recordings where applicable<br />-    Administer psychological and physiologic test procedures<br />Documentation &amp; Data Management<br />-    Provide volunteers with study-relevant documentation, diaries, and forms<br />-    Manage CRF corrections in coordination with quality management and assurance teams<br />-    Manage CRFs, source data storage, and archiving following study completion<br />-    Resolve data clarification queries promptly<br />-    Issue audit reports on internal and external quality audit findings<br /><u>Stakeholder Engagement</u><br />-    Cooperate with study monitors, including preparation for monitor visits and document review<br />-    Participate in study team sessions, study initiation meetings, and sponsor sessions<br />-    Communicate shift-to-shift study-relevant information to the team<br />-    Manage volunteer payments and incentives</p><p></p><p><b>Required Qualifications:</b><br /><u>Education</u><br />-    Completed nursing qualification (Registered Nurse/Nurse), MTA (Medical Technical Assistant), doctor&#39;s assistant, paramedic, or equivalent qualification<br /><u>Experience</u><br />-    Relevant experience in a hospital or medical/surgical setting<br /><u>Skills &amp; Competencies</u><br />-    Fluent German and good written and oral English proficiency<br />-    Proficient with Windows Office applications<br />-    Strong organizational and time management skills<br />-    Ability to work effectively under pressure<br />-    Flexibility with shift work (early, late, night shifts)<br />-    Availability for weekend and holiday work<br />-    Attention to detail and commitment to data accuracy<br />-    Strong communication and teamwork skills.</p>",
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        "descriptor": "Germany"
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      "descriptor": "Germany-Berlin-Haus 31"
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