About Johnson & Johnson At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive,
About Johnson & Johnson At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive,
About Johnson & Johnson At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter
About Johnson & Johnson At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter
JOB SUMMARY: Briefly state the objective of this position. JCS supports Japan Clinical Lead (JCL) activities in the development and execution of clinical development strategy for target indication(s) in assigned compound(s) to obtain regulatory approval in Japan. Based
About Johnson & Johnson At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter
About Johnson & Johnson At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive,
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Helping deliver life-changing therapies Our broad range of clinical development and analytical services enables Thermo Fisher Scientific customers to drive innovation and increase drug development productivity. Recognized for accelerating promising
Job Description Outbound managerとしてチームのリードをお任せします。倉庫オペレーション業務経験のある方、治験ビジネスにご興味のある方、将来的にキャリアを広げる方向性に興味のある方、英語を使った仕事に挑戦したい方など、ご応募をお待ち申し上げます。 Division Specific Information Clinical Trials Division (CTD) partners with pharmaceutical and biotech customers around the world to ensure the right patients get the right therapies in the right doses at the right time –
* Ensure the trial set up and the progress of the clinical studies under responsibility, in accordance with local regulations, Good Clinical Practices, internal procedures, technical protocols. 企業情報 * グローバル製薬 * オンコロジー 職務内容 * Support the Japanese development strategy
As a Senior Data Manager, you will lead a team to ensure high-quality data management in clinical trials, driving regulatory compliance and project success. This role offers impactful work and career advancement in a leading organization focused on
As the Observational Research Program Manager, you will spearhead efforts to utilize real-world evidence to support drug development and regulatory decisions. Your role will focus on advancing research methodologies while enhancing organizational capabilities. 企業情報 A leading
We are looking for a Data Architect Project Leader for an international pharmaceutical firm. You will manage and improve our Real-world Data (RWD) platform for the business. Client Details Our client is a global bio-pharmaceutical company
1. Objectives: In order to obtain high-quality pharmacokinetic (PK)/biomarker/antibody/pharmacogenomics (PGx) data from a clinical study, take charge of series of work concerning PK/biomarker/ antibody/PGx assay and oversight assay sites in order to execute these duties. In addition
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Career CategoryScientific Job Description Live What you will do Accountabilities Develop, implement and maintain an integrated site engagement and operational role at key/targeted sites in line with Global Development pipeline to support strategic global study strategy
Study Start Up Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to
JOB description To keep up and improve the local supply processes in Japan including roles and responsibilities of involved local and global functions as well as the SOP system which should be in line with global
Job description: 1. To keep up and improve the local supply processes in Japan including roles and responsibilities of involved local and global functions as well as the SOP system which should be in line with
臨床試験のデータマネジメント業務を担当しています。 新薬の承認を得るために必要となる臨床試験データの品質管理を責務としています。 さまざまな治療領域と臨床試験のすべてのフェーズを経験しており、国内外のお客様の試験をサポートするために、包括的なデータマネジメントソリューションを提供しています。 <業務内容> 治験データマネジメントチームのリードとして、DM業務のプロジェクトマネジメントをお任せします。 ・プロジェクトの新規立ち上げからデータベースロックまでの管理 ・タイムラインやシステム構築の提案 ・DMP(Data Management Plan)の作成やレビュー ・社外顧客や社内他部署とのコミュニケーションや調整 ・プロジェクトの進捗管理や予実管理 他 <勤務地> 品川/大阪 <必須> 以下すべての条件に合致する方 ・ データマネジメント 業務の経験が5年以上ある ・ データマネジメント のリード(責任者)としての業務経験がある ・社外顧客とのコミュニケーション経験がある <あれば尚可> ・Raveでのシステムの構築・運用の実務経験 ・英語で記載された文書を理解することができる ・英語でメールのやりとりができる <キャリアパス、特別な研修・サポート制度、働き方等> ・体系的なSOPやeLearningによる教育研修が充実しています。 ・入社直後は、OJTを通してプロジェクトをご経験頂きます。 ・産休、育休、時短勤務をサポートしています。 ・当部門では、ほとんどの社員が在宅で勤務しています。 ・充実した英語トレーニング・サポート体制によって、英語のスキルアップが図れます。 会社負担でGlobal English