リファイン すべてリセット
距離:
ソート
雇用主/採用担当者
掲載日
職種
雇用主/採用担当者
経験
給与の見積もり
すべてのフィルタ

Clinical Documentationの求人-榛原郡吉田町 - 67 Job Positions Available

67 / 1 - 20 求人
Leidos 求人

Looking for an opportunity to make an impact? The Leidos Federal Health Solutions division is looking for individuals who feel they have more to give, want to learn new skills, and be part of a team

Leidos  29日前
IQVIA 求人

Job Overview Manage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and is in accordance with standard operating procedures (SOPs), policies and

IQVIA  25日前
Boehringer Ingelheim 求人

Basic purpose of the job* The Head of Development Regulatory Affairs 1 or 2 has responsibility to develop and implement regulatory strategy for the assigned therapeutic areas (TAs) and exercises activities which include: Guide subordinates on

Boehringer Ingelheim  25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

Boehringer Ingelheim  25日前
Boehringer Ingelheim 求人

Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen Nippon

Boehringer Ingelheim  25日前
Boehringer Ingelheim 求人

Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen Nippon

Boehringer Ingelheim  25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

Boehringer Ingelheim  25日前
Boehringer Ingelheim 求人

Publication Strategy Manager パブリケーションストラテジーマネージャー Basic purpose of this job: 各疾患領域の戦略に沿った、研究データの適切適時なパブリケーション(論文公表・学会発表)を推進する役割です。 To define and execute the local publication plans in a strategic and compliant manner, considering the overarching HPBU and brand specific strategy and ensuring: - regular

Boehringer Ingelheim  25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
Real Staffing 求人

Job Opportunity: Pharmacovigilance Associate - Japan, Osaka About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. They are proud to foster an inclusive environment that drives innovation and excellence, and they welcome

Real Staffing  26日前
Real Staffing 求人

CRA

Job Opportunity: Clinical Research Associate I (CRA I) - Japan, Tokyo (Hybrid: Office/Remote) About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. They are proud to foster an inclusive environment that drives innovation

Real Staffing  26日前
Real Staffing 求人

About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. Proudly fostering an inclusive environment that drives innovation and excellence, the organization welcomes you to join its mission to shape the future of

Real Staffing  26日前
Real Staffing 求人

Job Opportunity: Senior Biostatistician Responsibilities * Ensuring that all statistical aspects of documentation pertaining to clinical programs and non-study activities meet required standards and are statistically accurate. * Influencing study design and analysis, and defending statistical approaches internally

Real Staffing  26日前
Real Staffing 求人

Job Opportunity: Project Manager, Laboratory - Japan, Tokyo (Hybrid: Office/Remote) About Our Client Our client is a world-leading healthcare intelligence and clinical research organization. Proudly fostering an inclusive environment that drives innovation and excellence, the organization welcomes

Real Staffing  26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  20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  20日前
IQVIA 求人

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 internal guidelines

IQVIA  20日前
Randstad Sourceright - Japan 求人

Key Accountabilities Country Quality System management Lead the implementation and maintenance of GxP quality system with respective operation units, the continues quality system implementation for competencies and related Quality documentation of GxP area: medical, pharmacovigilance, regulatory and

Randstad Sourceright - Japan  20日前
Boehringer Ingelheim 求人

Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen Nippon

Boehringer Ingelheim  19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  18日前

新しい機会を逃さないで!

確認メールの送信先

メールを確認し、リンクをクリックして求人情報の受信を開始します。

最新の求人情報を受け取ることができます。

clinical documentation 求人 全国 榛原郡吉田町

次も興味があるかもしれません:

Japanese

Clinical Trials

Matrix

Clinical Development

Therapeutic Areas

Pharmacovigilance

Feasibilities

Clinical Research

Clinical Operations

Risk Management

確認メールの送信先

メールを確認し、リンクをクリックして求人情報の受信を開始します。

すべてのフィルタ 申請する
ソート
雇用主/採用担当者