Basic Purpose of the Job Supports the complete clinical/pharmaceutical drug lifecycle process (research, development, market access, and market supply) by providing: Strategic planning and execution Data transformation Descriptive analytics Diagnostic analytics Predictive analytics Prescriptive analytics Work involves data from:
Basic Purpose of the Job Key contact partner in cultivating the power of data by means of: Data collection/curation, data review, data delivery Data standardization Process definition, testing and training Translate scientific requirements into technical specifications. Collect, ingest, structure, curate and
Job Overview: Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. PSI is a leading Contract Research Organization with more
Job title: Clinical Operations Study Country Lead (COSCL) Location: Tokyo, Japan About the job Our Team: We are seeking a highly motivated and experienced Clinical Operations Study Country Lead to support local clinical trial operations. The COSCL will be
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.
Basic Purpose of the Job Supports the complete clinical/pharmaceutical drug lifecycle process (research, development, market access, and market supply) through: Strategic planning and execution Data transformation Descriptive analytics Diagnostic analytics Predictive analytics Prescriptive analytics Works with data from: Clinical trials
Basic Purpose of the Job Key contact partner in cultivating the power of data through: Data collection/curation, data review and data delivery Data standardization Process definition, testing and training Responsibilities include: Translating scientific requirements into technical specifications Collecting, ingesting, structuring, curating
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, andsolutions are personal.Through our
Job Purpose The Clinical Scientist (CS) in Japan is responsible and accountable for clinical scientific outputs for assigned projects and studies in Japan. The CS will have accountability for approximately 2 - 4 projects (assets) at any one
Job Description 1. Objectives Responsible for clinical development of the assigned project in Japan under the supervision of the Japan Development Leader (JDL), who assumes responsibility for development of all projects in Japan in the respective therapeutic/disease
Job Purpose The Clinical Development Lead (CDL) in Japan is the single point of accountability for all clinical development activities for assigned asset(s). The CDL provides scientific and medical leadership to define and deliver Japan clinical strategy, drives innovation
General Information Job Advert Title: Clinical Site Manager Ⅲ（臨床開発モニター/ Site Monitor/ CRA） Location: Nihonbashi, Tokyo Division: Clinical Operations, Quantitative Sciences and China Development Employment Class: Permanent Description 【About Astellas】 Astellas is a global life sciences company committed to
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
Job title: PMS Planning and Management Specialist • Location: Tokyo, Japan - About the job As a PMS Planning and Management Specialist within our Regulatory Affairs team, youll help ensure the safety and integrity of new medicines by
Job Title: PMS Planning and Management Head • Location: Tokyo, Japan - About the Job As PMS Planning and Management Head within our Regulatory Affairs & Patient Safety team, youll lead a high-performing group responsible for shaping post-marketing
Basic Purpose of the Job The Clinical Program Leader assumes Clinical Development responsibilities supporting early or late development projects, reporting to the Associate Global Head or the Global Clinical Programme Team Leader. The Clinical Program Leader has a medical leadership
Job Description 医薬品開発プロジェクトにおけるプロジェクトマネジメントおよびアライアンスマネジメント業務 – プロジェクトマネジメントおよびアライアンスマネジメントのスキルや専門知識、一般的ビジネススキル、および疾患領域特異的な知識や経験を基に、部門横断的および戦略的視点からプロジェクトを推進する。 ・プロジェクトスコープの特定と開発戦略の立案を推進する。 ・開発戦略の実行状況やタイムライン等の進捗管理を行う。 ・リスクマネジメント、ステークホルダーマネジメントを遂行する。 ・ガバナンスとプロジェクトの接点となり、開発戦略の意思決定を推進する。 ・US本社プロジェクトマネージャーやチームメンバーと協働し、世界同時開発を推進する。 ・他社との協働にあたり、アライアンスマネジメントを遂行する ・特許等様々な観点から、製品の価値最大化に貢献する。 【必要なスキル・経験】 ・5年以上の製薬会社での勤務経験 ・3年以上のプロジェクトマネジメント（もしくはそれに相当する）経験 ・ビジネスレベルでの英語力 【尚可要件】 PMP (Project Management Professional) 資格 知的財産関連資格および実務経験 ※ Grade：P3 (Sr. Specialist)での募集ですが、ご経歴によりP2 (Specialist) やP4 (Associate Director)で採用する場合がございます。 Required Skills: Adaptability, Adaptability, Business Functions,