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as legal lead for digital, data and privacy agreements, along with Business Associate Agreements as required under HIPAA.... Legal Research: Stay updated on legal and regulatory developments in the medical device industry and provide recommendations... Apply Now

Associate Director of Regulatory Affairs-Chemistry, Manufacturing, and Controls (RA-CMC) in Japan will be responsible... for leading and providing Japan CMC regulatory support for the clinical and commercial product portfolio, which means managing... Apply Now

Job Summary : The Japan Clinical Monitoring team is growing, and we are seeking a full-time an Associate Director... : Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services... Apply Now

Job Summary The Japan Clinical Monitoring team is growing, and we are seeking a full-time an Associate Director... Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services... Apply Now

【募集Summary】 Sr Records Management(RM) Associateは、IQVIAにおけるTMF Managementにおいて、TMF におけるDocument Processing(Imaging QC...を産前産後休暇とする ■育児休業：子供が1歳2ヵ月に達するまでを限度とし、本人の申し出た期間休業可能（やむを得ない場合は3歳まで可） ■介護休業 ■女性特別休暇 IQVIA is a leading global provider of clinical... Apply Now

part. Responsible for developing staff(Senior Clinical Research Associate and Clinical Research Associate) capabilities... with clinical research 【能力 / Skill-set】 ＜必須 / Mandatory＞ Effective in leading, motivating and empowering others in order... Apply Now

and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It... material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development... Apply Now

about our company and new grads’ career opportunities at Medpace Japan. Clinical Research Associate (CRA) and other professional roles... will be provided should you be selected to attend. Responsibilities Clinical Research Associate (CRA) - join our growing team... Apply Now

Research Associate (iCRA)は主に施設選定後から、施設の治験薬搬入可能となるまでの期間で、治験施設立ち上げ担当者として初回申請に必要な文書の作成から申請手続きを専任で行います。iCRAが施...ーバル試験80％以上の世界的CRO／世界70の拠点に約18,000人の社員が在籍するグローバル企業／仕事とプライベートバランスがとれた働きやすい環境】 ■職務内容：【変更の範囲：会社の定める業務】 initiation Clinical... Apply Now

Research Associate (iCRA)は主に施設選定後から、施設の治験薬搬入可能となるまでの期間で、治験施設立ち上げ担当者として初回申請に必要な文書の作成から申請手続きを専任で行います。iCRAが施...ーバル試験80％以上の世界的CRO／世界70の拠点に約18,000人の社員が在籍するグローバル企業／仕事とプライベートバランスがとれた働きやすい環境】 ■職務内容：【変更の範囲：会社の定める業務】 initiation Clinical... Apply Now