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Regulatory Interactionsの求人-nakakoma District Showacho - 106 Job Positions Available

106 / 1 - 20 求人
Bristol Myers Squibb 求人

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.

Bristol Myers Squibb  27日前
Bristol Myers Squibb 求人

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.

Bristol Myers Squibb  27日前
Goldman Sachs 求人

Internal Audit – Asset Management Audit (Associate, Tokyo) What We Do As the third line of defense, Internal Audit’s mission is to independently assess the firm’s internal control structure, including the firm’s governance processes and controls,

Goldman Sachs  26日前
JPMorgan Chase & Co. 求人

Great exposure in the JPMorgan Asset Management business. Our Sales teams provide the best solution to the partner funds distributors helping them build stronger portfolios and best ideas. As a Vice President in Sales Support within

JPMorgan Chase & Co.  26日前

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,

Johnson And Johnson  26日前
Swiss Re 求人

Position Outline The Legal Counsel shall be working in the APAC Legal & Compliance team with primary focus in managing legal & compliance issues relating to Swiss Res operations in Japan, namely Swiss Re International SE,

Swiss Re  24日前
Abbvie 求人

企業概要 AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across

Abbvie  24日前
Boehringer Ingelheim 求人

Basic purpose of the job The manager of RRL JP provides strong leadership to develop and implement regulatory strategy for the assigned products/projects as RRL JP, and exercises activities which include: An integral member of the Regulatory Excellence

Boehringer Ingelheim  24日前
Boehringer Ingelheim 求人

Basic purpose of the job Delivers project management support to the asset team and next–level teams with the focus on asset strategy execution and asset progress. Coordinates the interactions with all key stakeholders, local and Global (including

Boehringer Ingelheim  23日前
AstraZeneca 求人

■ 職務内容 / Job Description Clinical Scientist (CS) is a clinical project lead with strong experience in multidisciplinary aspects of drug development and is accountable/responsible for generating clinical development strategy, designing clinical development options, and delivering

AstraZeneca  22日前
Amgen 求人

Career CategoryQuality Job Description Description Quality and Compliance oversight of External sites. Ensure External site activities are in alignment with applicable product CTA /Marketing Application. Key Responsibilities Serve as the main Quality point of contact related

Amgen  22日前
Amgen 求人

Career CategoryRegulatory Job Description Group Purpose Japan Regulatory Affairs provides leadership, expertise, and execution for the regulatory strategy to obtain and maintain clinical trial and marketing licenses for Amgen molecules in Japan in alignment with local business priorities

Amgen  22日前
Alexion Pharmaceuticals 求人

Principal Responsibilities ・Accountable as Regulatory Lead to develop and implement regulatory strategies for assigned product(s)/project(s) in Japan and accountable to provide regulatory advice to cross-functional strategies and associated deliverables according to business objectives. ・Lead the planning and conduct of

Alexion Pharmaceuticals  21日前
WTW 求人

The Business We know how companies can unlock potential through effective risk management. Our clients rely on us to craft strategies to quantify, mitigate, and transfer risk, taking advantage of our specialist industry experience and unparalleled

WTW  21日前

Responsible for executing the following basic MSL tasks under the guidance of his/her superior and the support of a senior MSL. • Responsible for building trust relationship with Key Individuals (KIs) in their therapeutic area and

Johnson And Johnson  21日前
Astellas Pharma 求人

General Information Job Advert Title: Clinical Trial Lead Location: Nihonbashi,Tokyo Division: Early Development Employment Class: Permanent Description Development, Early Development, Clinical operation, Clinical study 【募集の背景 / Purpose & Scope】 This position is accountable for the planning,

Astellas Pharma  20日前
Takeda 求人

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms

Takeda  18日前
Abbvie 求人

企業概要 AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across

Abbvie  17日前
Boehringer Ingelheim 求人

Basic purpose of the job To maximize sales and patients health of the own products on a short and long term basis by planning and executing marketing strategies successfully Accountabilities Ensure achievement of target sales, growth

Boehringer Ingelheim  17日前
Boehringer Ingelheim 求人

Basic purpose of the job Insight Analyst is responsible for supporting therapeutic area teams with medical insight management. The role involves ensuring proper recording of scientific insights, resolving technical issues with insight capturing platforms, and analyzing

Boehringer Ingelheim  16日前

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regulatory interactions 求人 全国 nakakoma district showacho

次も興味があるかもしれません:

Japanese

Clinical Development

Clinical Trials

Pharmaceutical Industry

Therapeutic Areas

Publications

Risk Management

Medical Affairs

Drug Development

Regulatory Requirements

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