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Clinical Documentationの求人-黒川郡大衡村 - 40 Job Positions Available

40 / 1 - 20 求人
Reckitt 求人

We are Reckitt そのチカラを自由に使え。 今の自分を超えていけ。 FREE YOUR POWER. PROGRESS YOURSELF. Home to the worlds best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the

Reckitt  10日前
Leidos 求人

The Leidos Military & Veterans Health Solutions Group is hiring a counselor for our PACAF and Marines Adolescent Support and Counseling Services (ASACS) program. This program implements a community-based adolescent support and counseling program for the

Leidos  9日前
Novo Nordisk 求人

Do you have a strong background in non-clinical activities? We are looking for a Non-Clinical Expert to join our team at Novo Nordisk. If you are ready to contribute to the development, submission, and approval of new drugs/devices,

Novo Nordisk  9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

We will use your ability to integrate/apply knowledge of global & Japanese regulations governing drug development to progressing Regenerons portfolio. This includes preclinical and clinical drug development programs, policies, and procedures. This is an exciting opportunity to

Regeneron  7日前
BeiGene 求人

About us BeiGene is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse

BeiGene  14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  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  21日前
Novartis 求人

Job Description SummaryThe SSO Associate Clinical Project Manager (aCPM) is accountable for the day-to-day planning, executing and reporting, (from first site initiation visit to and including study site close-out), of assigned Global Drug Development (GDD) studies in

Novartis  27日前
Novartis 求人

Job Description SummaryAccountable for the oversight and coordination of program and study level (re-)feasibility assessments in the country, in collaboration with program and/or trial feasibility teams, in compliance with Novartis processes, GCP, ICH and regulatory requirements.

Novartis  23日前

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

Johnson And Johnson  9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  13日前
IQVIA 求人

Job Overview Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and

IQVIA  16日前
Novartis 求人

Job Description Summary To manage business and operational activities of local regulatory writing (RW) to ensure timely production of high quality clinical documentation. To ensure compliance with global RW strategy and implementation of technical activities & strategies according

Novartis  6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  5日前
Astellas Pharma 求人

General Information Job Advert Title: Senior Scientist(Toxicologist) Location: Tsukuba, Ibaraki Division: Applied Research & Operations Employment Class: Permanent Description 【募集の背景 / Purpose & Scope】 This position has responsibility for non-clinical safety profiling and characterization of development candidates

Astellas Pharma  5日前
Astellas Pharma 求人

General Information Job Advert Title: Senior Manager, Technology and Data QA Location: Nihonbashi, Tokyo Division: Quality Assurance Employment Class: Permanent Description 【Purpose & Scope】 Responsible for managing and executing the Technology and Data Quality Assurance (TDQA)audit

Astellas Pharma  5日前
Astellas Pharma 求人

General Information Job Advert Title: DWH Architect – Azure AWS Data Warehouse Location: Nihonbashi, Tokyo Division: DigitalX Employment Class: Permanent Description 【About Astellas】 As part of the Astellas commitment to delivering value for our patients, our

Astellas Pharma  5日前
Astellas Pharma 求人

General Information Job Advert Title: Clinical Trial Associate (CTA) Location: Tokyo HQ (Nihonbashi) Division: Clinical Operations Employment Class: Permanent Description 【募集の背景 / Purpose & Scope】 In Clinical Operations Oncology, we work with domestic and international co-development partners and overseas

Astellas Pharma  5日前

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clinical documentation 求人 全国 黒川郡大衡村

次も興味があるかもしれません:

Japanese

Clinical Trials

Drug Development

Feasibilities

Clinical Development

Briefing

Risk Management

Conflict Resolution

Childcare

Standard Operating Procedure

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