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Clinical Trial Management Systemの求人-中央区 - 32 Job Positions Available

32 / 1 - 20 求人
Edwards Lifesciences 求人

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a

Edwards Lifesciences  17日前
Fortrea 求人

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 delivery

Fortrea  13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  13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  9日前
Boehringer Ingelheim 求人

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.

Boehringer Ingelheim  6日前
GSK 求人

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

GSK  4日前
GSK 求人

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

GSK  4日前
Astellas Pharma 求人

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

Astellas Pharma  4日前
PSI CRO 求人

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

PSI CRO  2日前
Sanofi 求人

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

Sanofi  2日前
Sanofi 求人

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

Sanofi  2日前
Fortrea 求人

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project

Fortrea  13日前
Fortrea 求人

Job Overview: Role is primary contact for investigative sites for site payments. Responsible for administering grant and non-grant payments in accordance with the site executed agreement. Summary of Responsibilities: Accountable for the overall payment management of assigned

Fortrea  13日前
Fortrea 求人

Job Overview: Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made

Fortrea  13日前
Johnson & Johnson 求人

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

Johnson & Johnson  26日前
Boehringer Ingelheim 求人

Basic Purpose of Job Manage case processing activities for Nippon Boehringer Ingelheim’s investigational and marketed products including case submission to Global Patient Safety and Pharmacovigilance (PSPV) and PMDA according to Boehringer Ingelheim (BI)’s internal procedure and

Boehringer Ingelheim  25日前
Fortrea 求人

Job Overview: At times working under the direction of a Project Director, the Senior Project Manager oversees and manages domestic, regional and/or global projects. Responsibilities typically include developing and managing project teams, communications, risk, scope, schedule,

Fortrea  24日前
AmerisourceBergen 求人

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on

AmerisourceBergen  18日前
Boehringer Ingelheim 求人

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

Boehringer Ingelheim  6日前
Syneos Health 求人

CRA II Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate

Syneos Health  3日前

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clinical trial management system 求人 全国 中央区

次も興味があるかもしれません:

Clinical Trials

Life Sciences

Therapeutic Areas

Site Management

Tracking Systems

Japanese

Informed Consent

Drug Development

Readiness

Regulatory Requirements

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