Clinical data management job offers in maharashtra

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  • Clinical Systems Tester - Veeva EDC | QNI422

    new GVR Infotek Kolhapur, Maharashtra  +3 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • (QGN-239) - Clinical Systems Tester - Veeva EDC

    new GVR Infotek Pune, Maharashtra

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • YOM-119 | Clinical Systems Tester - Veeva EDC

    new GVR Infotek Mumbai, Maharashtra

    ...workflows. Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP). Detail-oriented with strong documentation and communication skills
    19 h 43 minutes ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC - V621

    new GVR Infotek Nagpur, Maharashtra  +4 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • AE276 Clinical Systems Tester - Veeva EDC

    new GVR Infotek Amravati, Maharashtra  +10 locations

    ...workflows. Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP). Detail-oriented with strong documentation and communication skills
    19 h 50 minutes ago in Kitjob_in

    Report

  • [C445] Clinical Systems Tester - Veeva EDC

    new GVR Infotek Sangli, Maharashtra  +10 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC | (ZP662)

    new GVR Infotek Solapur, Maharashtra  +6 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC | [KV425]

    new GVR Infotek Thane, Maharashtra  +5 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC | [LHA415]

    new GVR Infotek Aurangabad, Maharashtra  +5 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC | HN864

    new GVR Infotek Dombivli, Maharashtra  +6 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    20 h 16 minutes ago in Kitjob_in

    Report

  • D653 | Clinical Systems Tester - Veeva EDC

    new GVR Infotek Kolhapur, Maharashtra  +6 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    20 h 25 minutes ago in Kitjob_in

    Report

  • O502 | Clinical Systems Tester - Veeva EDC

    new GVR Infotek Dombivli, Maharashtra  +6 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • (TV457) - Clinical Systems Tester - Veeva EDC

    new GVR Infotek Nagpur, Maharashtra  +5 locations

    ...workflows. Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP). Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC [GSW-721]

    new GVR Infotek Mumbai, Maharashtra  +2 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC [LH-356]

    new GVR Infotek Nagpur, Maharashtra

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC | [GKE-202]

    new GVR Infotek Dombivli, Maharashtra

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC [GL004]

    new GVR Infotek Amravati, Maharashtra  +7 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    20 h 39 minutes ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC [EGT873]

    new GVR Infotek Mumbai, Maharashtra  +7 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC (FLW-022)

    new GVR Infotek Dombivli, Maharashtra

    ...workflows. Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP). Detail-oriented with strong documentation and communication skills
    19 h 51 minutes ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC [W830]

    new GVR Infotek Thane, Maharashtra  +3 locations

    ...workflows. Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP). Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • [M-581] - Clinical Systems Tester - Veeva EDC

    new GVR Infotek Nagpur, Maharashtra  +7 locations

    ...workflows. Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP). Detail-oriented with strong documentation and communication skills
    19 h 57 minutes ago in Kitjob_in

    Report

  • [S360] - Clinical Systems Tester - Veeva EDC

    new GVR Infotek Pune, Maharashtra  +7 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • [I-856] - Clinical Systems Tester - Veeva EDC

    new GVR Infotek Nashik, Maharashtra  +7 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • [EU212] - Clinical Systems Tester - Veeva EDC

    new GVR Infotek Sangli, Maharashtra  +7 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

  • TZ420 Clinical Systems Tester - Veeva EDC

    new GVR Infotek Navi Mumbai, Maharashtra  +4 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    1 day ago in Kitjob_in

    Report

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Clinical data management job offers in maharashtra

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