Study manager (FSP)

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  "active_status": "active"
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  "location": {
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    "title": "Study manager (FSP)",
    "postedOn": "Posted 3 Days Ago",
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    "location": "China-Shanghai Shinmay",
    "postedOn": "Posted 3 Days Ago",
    "timeType": "Full time",
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    "startDate": "2026-06-17",
    "externalUrl": "https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/China-Shanghai-Shinmay/Study-manager--FSP-_R0000041734",
    "jobPostingId": "Study-manager--FSP-_R0000041734",
    "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><u>:</u> </p><p><b>General Accountabilities</b> </p><ul><li><p>Build and maintain engagement with Investigators, other site staff  in collaboration with other functions, to ensure trial speed and effective start up, conduct and close out. </p></li></ul><ul><li><p>Ability to manage studies and processes to agreed quality and timelines. </p></li></ul><ul><li><p>Ability to proactively identify &amp; mitigate risks around study/site level in study execution. </p></li></ul><ul><li><p>Knowledge of the clinical development process, understand concepts and principles of study design, and application to manage and run studies. </p></li></ul><p><b> </b></p><p><b>Compliance with Parexel standards </b> </p><p></p><ul><li><p>Comply with required training curriculum.  </p></li></ul><ul><li><p>Complete timesheets accurately as required.  </p></li></ul><ul><li><p>Submit expense reports as required.  </p></li></ul><ul><li><p>Update CV as required.  </p></li></ul><ul><li><p>Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable requirements.  </p></li><li><p>Previous experience in scientific and/or regulatory medical writing. </p></li><li><p>Strong Communication Skills </p></li></ul><p></p><p><b><u>Knowledge and Experience</u></b>:  </p><ul><li><p>Keen problem-solving skills. </p></li></ul><ul><li><p>Fluent in both oral and written English. </p></li></ul><ul><li><p>Fluent in host country language required.  </p></li></ul><ul><li><p>At least 5 years in clinical practices </p></li></ul><p></p><p><b><u>Education:</u></b> </p><ul><li><p>Minimum of BS/BA in a biomedical discipline or equivalent education/training is required </p></li></ul><p></p><p></p><p></p><p></p>",
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