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Statistician 気になる

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【HPBR】大手外資系医薬品メーカー/リモート可能 / HR Business Partner

募集要項

業務内容

■About the Department
Novo Nordisk is a global healthcare company with more than 100 years of innovation and supervision in diabetes care. This heritage has given us experience and capabilities that also enable us to help people defeat obesity, haemophilia, growth disorders and other serious chronic diseases.

The position of Statistician is to be in Tokyo, and report to Senior Director, Strategic Pharmacovigilance & Scientific Data Generation.

■The Position
As the Statistician, you will be accountable for all statistics within the designated projects/trials and optimize the clinical development plan statistically. You will complete the protocol, statistical analysis plans (SAP), data handling, clinical trial report (CTR), non-interventional study report (NSR), common technical document (CTD) and regulatory documents statistically. You will also drive Case Report Form (CRF), Trial Validation Plan (TVP), CTR data flow plan input, CTR/NSR workflow plan, Statistical Programming Specification (SPS) as well as perform statistical analysis and programming of output according to specification.

・Other tasks include, but are not limited to:
Drive trial outline (TO) development including sample size calculation, protocol development including statistical section of protocol. Support to derived programming according to industry standards. Interpret trial results and present results for the project and upper management. Day-to-day trial execution and coordination within the trial stats team. Ensure project statistical programming specification input and statistical input to design of trial.
Do presentation and negotiation of clinical development program at meetings with regulatory authority/Pharmaceuticals and Medical Device Agency (PMDA). Develop submission document(s), and post-submission activities to achieve regulatory approval and optimal labelling to allow the successful launch of the drug.
Share better practices and increase awareness of statistics within the designated projects and Clinical Medical Regulatory development division. Act a part of the standardization and globalization of the statistical activities.
Be responsible for continuous development of own skills (statistical knowledge, English communication skill, needed training and education) according to individual development plan (IDP).
Keep Headquarters up to date on PMDA requirements on electronic data submission, review e-data consultation documents by checking e-data to submit to PMDA and coordinate e-data consultation.

語学力


・Fluent in English (written and spoken) to be able to attend online meetings (once/week) and email communications (several times/day) in English.

年収

700万~1100万

給与

年俸制
賞与 年2回
増員

雇用形態

正社員

勤務地

東京都

通勤交通費

全額支給

休日

年間休日122日
【休日】


祝日
【休暇】
年末年始休暇
【休暇メモ】
■慶弔休暇、育児休業、介護休業
■積立休暇制度
■年次有給休暇(初年度12日 最高20日)

福利厚生

各種社会保険完備

営業手当
日当手当(営業外勤日3000円~/日)■昇給年1回(4月)
■財形貯蓄
■企業年金
■退職金
■慶弔見舞金制度
■研修制度
■借上社宅制度
■クラブ活動、保養所 ほか

※借り上げ社宅制度:補助(6.5万円~11万円)エリアと世帯数によって金額が異なります。

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企業情報

事業内容

医療用医薬品、医療機器の開発、輸入・製造、販売

業種分類

メディカル/医薬品メーカー

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  • 北海道・東北
  • 関東
  • 上信越・北陸
  • 東海
  • 関西
  • 中国
  • 四国
  • 九州・沖縄
  • 海外
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