Clinical Pharm Lead

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  "last_changed_at": "2026-06-20T08:53:10.525Z",
  "active_status": "active"
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  "language": "en",
  "location": {
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    "city": null,
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    "country": "China",
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{
  "list_job": {
    "title": "Clinical Pharm Lead",
    "postedOn": "Posted 4 Days Ago",
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    "title": "Clinical Pharm Lead",
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      "descriptor": "China"
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    "jobReqId": "R0000041707",
    "location": "China-Shanghai Shinmay",
    "postedOn": "Posted 4 Days Ago",
    "timeType": "Full time",
    "logoImage": {
      "alt": "Parexel",
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    "startDate": "2026-06-16",
    "externalUrl": "https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/China-Shanghai-Shinmay/Clinical-Pharm-Lead_R0000041707",
    "jobPostingId": "Clinical-Pharm-Lead_R0000041707",
    "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>Plans and directs clinical pharmacology components of clinical programs (including clinical development plan and medicine plan) and studies (including design, synopsis preparation and reporting). </p></li><li><p>Works with multifunctional study team to design, deliver and report the assigned clinical pharmacology studies and has overall scientific accountability for the designated studies. </p></li><li><p>Accountable for the development and implementation of a clinical modeling and simulation plan based on agreed-upon best practices (i.e. model-informed drug development). </p></li><li><p>Responsible for use of quantitative methods to integrate knowledge of pharmacokinetics, pharmacodynamics, patient characteristics and disease states to optimize doses, dosage regimens and study designs throughout clinical drug development. </p></li><li><p>Responsible for appropriate summarization and interpretation of results of pharmacokinetic/pharmacodynamic (PK-PD) analyses with respect to their impact on development and clinical use of drugs</p></li></ul><p></p><p><b>Compliance with Parexel standards </b> </p><ul><li><p>Comply with required training curriculum.  </p></li><li><p>Complete timesheets accurately as required.  </p></li><li><p>Submit expense reports as required.  </p></li><li><p>Update CV as required. </p></li><li><p>Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable requirements.  </p></li></ul><p></p><p><b><u>Skills:</u></b> </p><ul><li><p>Demonstrates thorough understanding of the following: 1) principles of PK, PK-PD and pharmacology relevant to drug candidates; 2) other relevant scientific disciplines, including drug metabolism, drug transport, formulation sciences, biopharmaceutics, pathophysiology<u> </u>and therapeutics; and 3) quantitative modeling and simulation principles. </p></li></ul><p></p><p><b><u>Knowledge and Experience:  </u></b></p><ul><li><p>Keen problem-solving skills. </p></li><li><p>Fluent in both oral and written English. </p></li><li><p>Fluent in host country language required.  </p></li></ul><p></p><p><b><u>Education:</u></b> </p><ul><li><p>Fluent in host country language required.  </p></li></ul>",
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      "descriptor": "China-Shanghai Shinmay"
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