Project Assistant (m/f/d)

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  "last_changed_at": "2026-06-10T07:49:47.496Z",
  "active_status": "deleted"
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{
  "language": "en",
  "location": {
    "raw": "Berlin",
    "city": null,
    "region": null,
    "country": "Berlin",
    "is_remote": false,
    "confidence": 0.8
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  "launch_scope": {
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    "included": true,
    "location": {
      "raw": "Berlin",
      "city": null,
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      "country": "Berlin",
      "is_remote": false,
      "confidence": 0.8
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    "countries": [
      "Berlin"
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{}

{
  "id": "1662299",
  "name": "Project Assistant (m/f/d)",
  "office": "Berlin",
  "keywords": [],
  "schedule": "full-time",
  "createdAt": "2024-08-05T09:35:02+00:00",
  "seniority": "entry-level",
  "department": "CSG",
  "occupation": "general_and_other_r_and_d_and_science",
  "subcompany": "Clinische Studien Gesellschaft mbH",
  "employmentType": "permanent",
  "jobDescriptions": [
    {
      "name": "About us",
      "value": "<div style=\"text-align:justify;\"><strong>Clinische Studien Gesellschaft (CSG)</strong> is a renowned full-service contract research organisation based in Berlin. We specialise in conducting clinical trials and observational studies throughout Europe for drugs, medical devices and digital health applications in all indication areas. As the CRO of the IGES Group, we tap into a broad spectrum of real-world data. We also conduct research on behalf of our clients on the topics of utilisation, medical need, patient preferences and clinical pathways.</div><br>To strengthen and support our team in the field of clinical research, we are looking for the next possible date for a <strong>Project Assistant (m/f/d).</strong>"
    },
    {
      "name": "Your mission",
      "value": "<ul><li><div style=\"text-align:justify;\">Collaboration in the preparation of calculations and offers</div></li><li><div style=\"text-align:justify;\">Correspondence with authorities, study centres and clients</div></li><li><div style=\"text-align:justify;\">Creation and maintenance of the Trial Master File (TMF) and Investigator Site File (ISF)</div></li><li><div style=\"text-align:justify;\">Participation in the creation and review of study documents</div></li><li><div style=\"text-align:justify;\">Collaboration in quality management projects</div></li><li><div style=\"text-align:justify;\">Submissions of clinical studies to ethics committees</div></li><li><div style=\"text-align:justify;\">Maintenance of study data in databases, creation and dispatch of status reports</div></li><li><div style=\"text-align:justify;\">Ordering study material and sending study documents</div></li><li><div style=\"text-align:justify;\">Preparation and follow-up of meetings (incl. taking minutes)</div></li></ul>"
    },
    {
      "name": "Your profile",
      "value": "<ul><li><div style=\"text-align:justify;\">University degree in the medical-technical/medical-documentary or scientific field or comparable training</div></li><li><div style=\"text-align:justify;\">Initial experience in the field of medical contract research or in the implementation studies is an advantage</div></li><li><div style=\"text-align:justify;\">Experience in pharmacovigilance desirable</div></li><li><div style=\"text-align:justify;\">Knowledge of regulatory processes and guidelines (e.g. ICH-GCP) desirable</div></li><li><div style=\"text-align:justify;\">Very good organisational skills and flexibility</div></li><li><div style=\"text-align:justify;\">Strong communication skills and a confident demeanour</div></li><li><div style=\"text-align:justify;\">Independent, reliable and detail-orientated way of working</div></li><li><div style=\"text-align:justify;\">Experienced with MS Office</div></li><li><div style=\"text-align:justify;\">Very good written and spoken German and English skills</div></li></ul>"
    },
    {
      "name": "Our offer",
      "value": "<ul><li><div style=\"text-align:justify;\">Entry-level position in clinical research processes with the opportunity to quickly assume your own responsibilities</div></li><li><div style=\"text-align:justify;\">Permanent employment and flat hierarchies</div></li><li><div style=\"text-align:justify;\">A pleasant working environment in the centre of Berlin</div></li><li><div style=\"text-align:justify;\">30 days holiday plus Christmas Eve and New Year's Eve off</div></li></ul>"
    },
    {
      "name": "contact information",
      "value": "<div style=\"text-align:justify;\">If this role appeals to you, we look forward to receiving your detailed application documents (cover letter, CV</div><div style=\"text-align:justify;\">and references) stating your salary expectations and earliest possible starting date via the application form or at</div><div style=\"text-align:justify;\"><a href=\"mailto:[email protected]\">[email protected]</a> . For further information, please contact Ms Antonia Kunz (030/230 809 211).</div>"
    }
  ],
  "occupationCategory": "r_and_d_and_science",
  "recruitingCategory": "CSG_Standard"
}