Biostatistician/Senior Biostatisticianの求人情報なら転職エージェントJAC

求人情報

Biostatistician/Senior Biostatistician

  • 転勤なし
  • 週休二日制
  • 外資
求人番号

NJB1031412

[無料]転職サポートのお申し込み

会社名 外資製薬メーカー <業種:メディカル・バイオ - 製薬>
職種

メディカル・バイオ-統計解析

雇用形態 正社員(期間の定めなし)
勤務地 東京都
仕事内容

<KEY TASKS & RESPONSIBILITIES>

-Functional Tasks

・As a trial biostatistician for statistically routine clinical trials, with limited direction provide statistical input for concept sheet/protocol/CRF development (e.g., trial design; sample size estimation for the most efficient and practical design; patient randomization; accurate, logical, clear, concise and thorough statistics section; effective CRF specifications to collect data specified in the protocol), write medical and statistical supervision plans, write statistical analysis plans, provide analysis dataset specifications, and perform statistical analyses.

・As a trial biostatistician for statistically complex clinical trials, with direction provide statistical input for concept sheet/protocol/CRF development, write medical and statistical supervision plans, write statistical analysis plans, provide analysis dataset specifications, and perform statistical analyses.

・For integrated safety and efficacy summaries for regulatory submissions, with direction write statistical analysis plans and perform statistical analyses.

・For statistically routine clinical trials, with limited direction write comprehensive statistical methods sections for the clinical trial reports; review and co-author these reports ensuring the accuracy of the statistical interpretation.

・For statistically complex clinical trials, with direction write comprehensive statistical methods sections for the clinical trial reports; review and co-author these reports ensuring the accuracy of the statistical interpretation.

・May validate statistical output as required.

・Provide statistical support for manuscripts and review manuscripts for accurate statistical interpretation.

・Participate effectively on clinical trial teams.

・With direction, plan, communicate, and implement the surveillance of the statistical activities performed by a Contract Research Organization.

・Exhibit routine and complex problem solving skills.

・Keep abreast of statistical developments.

・Communicate routine and complex statistical concepts and results to non-statistical internal and external colleagues in a clear, concise, focused and articulate manner.

・Understand and follow all Global Biostatistics WIs/SOP as well as any other relevant WIs/SOPs

-Managerial Tasks


■休日:年末年始 完全週休二日制

求める経験、能力
年齢制限の理由

・Preferably at least 3 years experience in the Pharmaceutical/Biotechnology industry in clinical development

・Working SAS knowledge

・Knowledge of relevant regulatory guidelines applicable to clinical development

・Familiarization with or ability to develop an understanding of relevant therapeutic areas


■職種未経験者:不可

年収 900万円 - 1200万円
語学力
英語力: 
中級

ご経験・スキルを考慮したうえで、非公開求人も含めた最適な求人のご紹介もいたします。
下記ボタンよりお申し込みのうえ、キャリアコンサルタントにご相談ください。
※既に当社にご登録いただいている方はこちらをご覧ください。


[無料]転職サポートのお申し込み

新規登録


ページの先頭へ戻る