Regulatory Officer (Clinical Trial Submissions) job opportunity at PSI CRO.

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Date2026-04-07T14:03:15.366Z bot
PSI CRO Regulatory Officer (Clinical Trial Submissions)
Experience: General
Pattern: Full-time
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degreeGeneral
loacation Almaty, Almaty Region, Kazakhstan
loacation Almaty, Almaty..........Kazakhstan
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Job DescriptionJoin our team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products in Kazakhstan, while taking a step further in your professional career.Office-based in AlmatyYou will:Prepare clinical trial submission dossiers for Regulatory and Ethics Authorities, including Import and Export license applicationsCommunicate with regulatory authorities, ethics committees, project teams and vendors on regulatory-related mattersReview translations of essential documents subject to clinical trial submissionTrack the regulatory project documentation flowReview documents to greenlight IP release to sitesManage safety reporting to authoritiesDeliver regulatory training to project teamsAssist with feasibility research and business development requests

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