Clinical Trial Assistant_ Digital (FSP)

{
  "content_hash": "273311e556755b228c618f9d3f5c6e1bb7f767a6954c236034488c8705b80679",
  "source_hash": "ecfd16e7b697096949b1a599dbe232182d2fd87f4a67db1b95adf8eed7c4b468",
  "last_changed_at": "2026-06-06T09:44:42.579Z",
  "active_status": "active"
}

{
  "language": "en",
  "location": {
    "raw": "China-Beijing",
    "city": null,
    "region": null,
    "country": "China",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-06T09:44:41.884Z",
  "launch_scope": {
    "reason": "workday_production_catalog",
    "included": true,
    "location": {
      "raw": "China-Beijing",
      "city": null,
      "region": null,
      "country": "China",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "China"
    ]
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": null,
  "salary_currency": null
}

{}

{
  "list_job": {
    "title": "Clinical Trial Assistant_ Digital (FSP)",
    "postedOn": "Posted Today",
    "bulletFields": [
      "R0000041759"
    ],
    "externalPath": "/job/China-Beijing/Clinical-Trial-Assistant_R0000041759-1",
    "locationsText": "China-Beijing"
  },
  "detail_errors": [],
  "detail_job_posting_info": {
    "id": "7e84cc8559e21000ee9a5a5db70d0000",
    "title": "Clinical Trial Assistant_ Digital (FSP)",
    "posted": true,
    "country": {
      "id": "6cb77610a8a543aea2d6bc10457e35d4",
      "descriptor": "China"
    },
    "canApply": true,
    "jobReqId": "R0000041759",
    "location": "China-Beijing",
    "postedOn": "Posted Today",
    "timeType": "Full time",
    "logoImage": {
      "alt": "Parexel",
      "src": "/wday/cxs/parexel/Parexel_External_Careers/sidebarimage/2d66767fe70110050ff90d0dbd4f0000"
    },
    "startDate": "2026-06-06",
    "externalUrl": "https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/China-Beijing/Clinical-Trial-Assistant_R0000041759-1",
    "jobPostingId": "Clinical-Trial-Assistant_R0000041759-1",
    "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><b><u>Key Accountabilities</u></b></p><p><b>Project Support</b></p><ul><li><p>Requests payments in Ariba Category Management (ACM)/ Ariba for study</p></li><li><p>related cost</p></li><li><p>Updates the trial and site information as necessary in Corporate Clinical Trial</p></li><li><p>Registry (CCTR) in a timely manner</p></li><li><p>Attends appropriate training programs and project teleconferences as</p></li><li><p>applicable</p></li><li><p>Maintains the study status tracking and provides analysis report to Study</p></li><li><p>Manager (SM)</p></li><li><p>Assists SM on study budget control by timely tracking and reporting of actual</p></li><li><p>cost and forecast drafting</p></li><li><p>Coordinates Clinical Study Agreement approval to ensure site initiation on</p></li><li><p>Time</p></li></ul><p><b>Study Start-Up</b></p><ul><li><p>Supports and coordinates the clinical trial application for amendment and</p></li><li><p>progress report to ethics committee and regulatory authority, if applicable,</p></li><li><p>and obtain approval within required timeline</p></li><li><p>Coordinates and applies for export/ import license of, lab kits, equipment,</p></li><li><p>and specimen, if applicable</p></li><li><p>Supports for preparations of site initiation packages (e.g. Site Master File</p></li><li><p>(SMF))</p></li><li><p>Organizes investigator meeting</p></li></ul><p></p><p><b>Study Conduct</b></p><ul><li><p>Supports and coordinates the clinical trial application for amendment and</p></li><li><p>progress report to ethics committee and regulatory authority, if applicable,</p></li><li><p>and obtain approval within required timeline</p></li><li><p>Maintains/ develops local tracking spreadsheets for study-related</p></li><li><p>documents, data, tasks, and activities, as applicable</p></li><li><p>Assists Clinical Research Associate (CRA) for the responsibility of tracking,</p></li><li><p>distribution, and filling of clinical trial documents/ information (eg. Suspected</p></li><li><p>undefined</p></li><li><p>Forms (CRFs), DCFs) with quality review for accuracy and completeness</p></li></ul><p></p><p><b>Other responsibilities of the CTA</b></p><ul><li><p>Supports SMs/ CTA Lead for quality improve related initiatives</p></li><li><p>Assists in preparation of newsletters and other study-related documents</p></li><li><p>Complies with client Policies, SOPs &amp; IGs and local regulations during various projects related transactions</p></li><li><p>Takes Subject Matter Expert (SME) role and provides training to CRA/ SM regularly</p></li><li><p>Ensures Metrics Compliance pertaining to CTA role</p></li><li><p>Provides back-up coverage for other CTAs as necessary</p></li><li><p>Mentors new CTA when applicable</p></li><li><p>Supports CTA lead for production and tracking of trial metrics measurements</p></li><li><p>Supports SM for coordinating with sites for finalizing budget worksheets and contractual agreements</p></li><li><p>Maintains and ensures the availability of inventory for all non-drug supplies</p></li><li><p>Provides logistic and administrative support to project teams</p></li><li><p>Assists on SUSAR package preparation for Ethics Committee and regulatory authority, if applicable</p></li></ul><p><b>Compliance with Parexel standards</b></p><ul><li><p>Complies with required training curriculum</p></li><li><p>Completes timesheets accurately as required</p></li><li><p>Submits expense reports as required</p></li><li><p>Updates CV as required</p></li><li><p>Maintains a working knowledge of and comply with Parexel processes, ICH[1]</p></li></ul><p></p><p><b><u>Skills:</u></b></p><ul><li><p>Proficiency in basic Computer Literacy (e.g. Microsoft word, Excel and PowerPoint)</p></li><li><p>Proficient in Chinese, good English skills in writing and reading</p></li><li><p>Good interpersonal skills, good at communication</p></li><li><p>A flexible attitude with respect to work assignments and new learning, quickly-learning</p></li><li><p>Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail</p></li><li><p>Willingness to work in a matrix environment and to value the importance of teamwork</p></li></ul><p><b><u>Knowledge and Experience:</u></b></p><ul><li><p>Knowledge of ICH GCP and local regulations is preferred</p></li><li><p>Experience in clinical trial administration is preferred</p></li><li><p>Experience in management of clinical trial and/ or regulatory documents is preferred</p></li><li><p>Knowledge of application used in the clinical trials is preferred</p></li></ul><p><b><u>Education:</u></b></p><ul><li><p>Science background is preferred</p></li><li><p>High or secondary School diploma/ certificate or above, University Graduate is preferred</p></li></ul>",
    "questionnaireId": "8a4ea2a2118710014cce04690bac0000",
    "jobPostingSiteId": "Parexel_External_Careers",
    "includeResumeParsing": true,
    "jobRequisitionLocation": {
      "country": {
        "id": "6cb77610a8a543aea2d6bc10457e35d4",
        "alpha2Code": "CN",
        "descriptor": "China"
      },
      "descriptor": "China-Beijing"
    }
  }
}