Clinical data management job offers in maharashtra

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  • [WHH052] Clinical Systems Tester - Veeva EDC

    new GVR Infotek Amravati, Maharashtra

    ...workflows. Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP). Detail-oriented with strong documentation and communication skills
    15 h 42 minutes ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC | (ZP662)

    new GVR Infotek Solapur, 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 (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
    15 h 27 minutes ago in Kitjob_in

    Report

  • [S360] - Clinical Systems Tester - Veeva EDC

    new GVR Infotek Pune, Maharashtra  +9 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  +1 Location

    ...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  +1 Location

    ...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

  • [XIT-542] - Clinical Systems Tester - Veeva EDC

    new GVR Infotek Thane, 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

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

    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
    15 h 33 minutes ago in Kitjob_in

    Report

  • [EU212] - Clinical Systems Tester - Veeva EDC

    new GVR Infotek Sangli, 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

  • Clinical Systems Tester - Veeva EDC | [OJ-187]

    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

  • D653 | Clinical Systems Tester - Veeva EDC

    new GVR Infotek Kolhapur, Maharashtra  +8 locations

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

    Report

  • O502 | Clinical Systems Tester - Veeva EDC

    new GVR Infotek Dombivli, Maharashtra  +8 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

  • A261 | Clinical Systems Tester - Veeva EDC

    new GVR Infotek Solapur, Maharashtra  +8 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

  • PI-863 | Clinical Systems Tester - Veeva EDC

    new GVR Infotek Thane, 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

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

    new GVR Infotek Nashik, 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

  • Clinical Systems Tester - Veeva EDC - JL199

    new GVR Infotek Mumbai, 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 - N-528

    new GVR Infotek Thane, 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 | (UO515)

    new GVR Infotek Pune, Maharashtra  +2 locations

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

    Report

  • Clinical Systems Tester - Veeva EDC | (K743)

    new GVR Infotek Nashik, 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 Y972

    new GVR Infotek Navi Mumbai, Maharashtra  +10 locations

    ...workflows Understanding of clinical trial regulatory requirements (21 CFR Part 11, GxP) Detail-oriented with strong documentation and communication skills
    15 h 32 minutes ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC NI96

    new GVR Infotek Pune, 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 [EGT873]

    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
    1 day ago in Kitjob_in

    Report

  • Clinical Systems Tester - Veeva EDC | BW-907

    new GVR Infotek Dombivli, 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 (LN360)

    new GVR Infotek Nashik, 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 - [OG115]

    new GVR Infotek Aurangabad, 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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