コンプライアンスマネジャー

募集要項

• こだわり条件

  設立50年以上 語学（英語）を生かす 残業月20時間以内 年間休日120日以上 土日祝日休み

• 仕事内容

  ■Accountabilities for company compliance management
  ・ To be familiar with the rules in the pharmaceutical industry and advises all departments in business from the viewpoint of legal affairs and compliance.
  ・ Bridging the Global SOP and regional rules to create and update the appropriate SOP for Nihon Servier.
  ・ Catching trends in rule changes at authorities and industry groups promptly and reflect them in the internal SOP.
  ・ Audit and supervise information provision activities for internal and external stakeholders.
  ・ Participate in the in house approval flow and examine each project from the viewpoint of compliance.
  ・ Create a violation prevention program by actively verifying in house compliance violations.
  Perform regular verification report to management and prevent recurrence by the program.
  ・ Conduct regular compliance training for internal companies and partner companies in
  collaboration with the internal training department.
  ・ Requesting advice from external advisors for maintaining appropriate compliance within the company.
  
  ■Medical information management
  ・ Create or review materials appropriate for information provision activities based on the product material creation rules instructed by Japanese authorities and HQ.
  ・ Be familiar with the information about company product and provide scientific advice to external and internal stakeholders.
  ・ Verify scientific evidence from in house materials and articles. Reflect appropriate
  information on sales and medical materials.
  ・ Support Field Medical activities by providing appropriate information for medical activities based on the latest evidence and guidelines announced at academia and societies.
  ・ Support for publication of papers written in house or by the Investigator.
  ・ Properly provide information according to information required from external stakeholders （Q A at call center and reception of external complaints regarding information provision activities and their response）.
  
  ■Other Duties
  ・ Multip…

• 職種分類

  管理部門 ＞ 管理部門 ＞ 法務・知財・特許

• 業種分類

  医薬・バイオ

• 応募条件

  【必須要件】
  ・製薬業界でのコンプライアンス業務経験
  ・英語ビジネスレベル

• 年収

  1000万円～1900万円
  1000万円 - 1900万円

• ポジション

  メンバー

• 雇用形態

  正社員

• 勤務地

  東京都

• 勤務時間

  09:15 ～ 17:15

• 休日・休暇

  【有給休暇】12
  【休日】完全週休二日制
  土
  日
  祝日
  GW
  夏季休暇
  年末年始
  【有給休暇】試用期間中は毎月1日付で1日付与、試用期間終了翌月1日付で4～20日間付与。
  ※年間付与日数は入社月により変動のため詳細はオファー時に通知

• 福利厚生

  【通勤手当】全額支給
  【社会保険】健康保険
  厚生年金
  雇用保険
  労災保険
  

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