Regulatory Affairs Associate

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  "last_changed_at": "2026-06-04T10:12:20.161Z",
  "active_status": "active"
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  "location": {
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    "region": null,
    "country": "India",
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    "confidence": 0.8
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  "inferred_at": "2026-06-04T10:12:19.574Z",
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    "location": {
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    "countries": [
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  "remote_policy": "remote",
  "salary_period": null,
  "workplace_type": "remote",
  "salary_currency": null
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    "location": "India-Bengaluru-Remote",
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    "timeType": "Full time",
    "logoImage": {
      "alt": "Parexel",
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    "startDate": "2026-06-04",
    "externalUrl": "https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/India-Bengaluru-Remote/Regulatory-Affairs-Associate-Annual-report---Renewals-Biologics-_R0000038455",
    "jobPostingId": "Regulatory-Affairs-Associate-Annual-report---Renewals-Biologics-_R0000038455",
    "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>Regulatory Affairs Associate </b></p><p></p><p>2 to 4 years of experience in Regulatory Affairs-CMC, should be willing to work in EU Shifts.</p><p>• To understand the regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions.</p><p>• Support authoring Annual reports/Renewal experience US/ EU/Brazil/LATAM/China.</p><p>• Liaise closely with cross-functional members with aligned product responsibilities.</p><p>• Knowledge of change evaluation according to country guidelines</p><p>• Experience in managing lifecycle activities in the EU markets would be preferrable</p><p>• Knowledge of CTD guidelines</p><p></p>",
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