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Clinical Documentationの求人-三重郡朝日町 - 42 Job Positions Available

42 / 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  9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  8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  8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  8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  6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  13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  3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  20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  26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  22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  12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  12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  15日前
CSL 求人

Position Purpose: The Regulatory Strategy Group Manager is a key leadership position in Japan Regulatory Affairs (RA) who contributes to achieve organizational vision and goals aligning with the strategic objectives of Global Regulatory Affairs (GRA) and

CSL  10日前
CSL 求人

Position Purpose: Senior Regularory Strategy Expert is responsible for all regional regulatory strategic and operational tasks for a range of development products/projects in the assigned TAs in Japan. The Senior Regularory Strategy Expert also provides technical

CSL  10日前
Ferring Pharmaceuticals 求人

Job Description: Key responsibilities: Liaises and supports development of KEEs Provides high quality medical and scientific support/communications to internal and external customers (e.g. advisory board meetings, training courses/workshops together with KEEs, support of speakers with presentations

Ferring Pharmaceuticals  2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  5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  5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

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clinical documentation 求人 全国 三重郡朝日町

次も興味があるかもしれません:

Japanese

Clinical Trials

Microsoft Office

Logistics

Drug Development

Clinical Development

Briefing

Risk Management

Feasibilities

Standard Operating Procedure

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