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過去7日間の求人情報

Pharmaceutical Industryの求人-駿東郡小山町 - 122 Job Positions Available

122 / 41 - 60 求人
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

Novo Nordisk  16時間前
Alexion Pharmaceuticals 求人

This is what you will do: The Launch Planning Lead will drive projects, generate insights, and make recommendations that will enable compliant, efficient, and effective execution of product launch preparation across Alexion’s portfolio to support successful

Alexion Pharmaceuticals  17時間前
BeiGene 求人

BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our

BeiGene  16時間前
BeiGene 求人

BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our

BeiGene  16時間前
Novo Nordisk 求人

Are you interested in improving the lives of millions of people, contributing to a company that works with innovation and is a pioneer in addressing the unmet medical needs? Do you have an innovative mindset to

Novo Nordisk  16時間前
GSK 求人

職務の目的および主な業務内容 Job Purpose & Key Responsibilities VEO Expertは、担当品目のValue Evidence Planの作成および実行に責任を持ちます。Evidence needsおよびGapを評価し、製品価値を高めるための最も適切な試験計画を組織横断チームにて立案し、提案していきます。 VEO Expert contributes to develop Japan Value Evidence Plan (J-VEP) of the assigned products. VEO Expert plan, implement and deliver high quality, scientifically robust research

GSK  16時間前
Santen 求人

企業概要 Santenは、眼科医療に特化した130年の歴史を持つ製薬企業です。日本発のグローバル企業として60カ国以上に拠点を持ち、目の健康のために様々な革新的な治療法とデジタルソリューションを提供し、世界中の人々の視覚に関わる社会問題に取り組んでいます。 求人内容 Manage contract and monitor the progress of all licensing relationships. This includes(i) maintaining good relationship with license partners and thus open the possibility of improvement/modification of terms, access to portfolio additions, etc, (ii)

Santen  16時間前
ERM 求人

About ERM Sustainabilityis our business. As the largest global pure play sustainability consultancy, ERM partners with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today

ERM  16時間前
Alexion Pharmaceuticals 求人

This is what you will do: The Medical Affairs Associate Medical Lead prepares a medical plan, which serves as the basis of medical activities of Alexion Pharma GK (AP-J) as a whole, and carries it out

Alexion Pharmaceuticals  16時間前
Michael Page 求人

Take lead in CMC RA activities for the business in regulatory strategy/maintenance to obtain and maintain regulatory approval. Contribute and support the CMC RA organization both domestically and overseas members Client Details * Global Pharmaceutical company specializing

Michael Page  10時間前
Michael Page 求人

Lead in QA activities to ensure effective compliance at the site. Establish and maintain effective QMS. Client Details * One of the top global bio pharmaceutical companies in the industry * Rich development pipeline leading in oncology, cardiovascular,

Michael Page  10時間前
Michael Page 求人

Take lead in quality activities to ensure effective compliance. Manage QMS and other quality claims. Client Details * Global pharmaceutical company specializing in innovative treatment for oncology, urology, and auto-immune areas. * Rich development pipeline for new

Michael Page  10時間前
Michael Page 求人

Leverage your fluency in Japanese and business-level English to develop and manage high-quality proposals for global clinical research projects. Contribute to groundbreaking medical advancements in a dynamic, collaborative environment while enjoying competitive compensation and professional growth

Michael Page  10時間前
Michael Page 求人

As Head of Pharmacovigilance, the role entails leading safety monitoring efforts for pharmaceutical products, ensuring regulatory compliance, and managing a team of professionals in these responsibilities. Client Details The organization focuses on providing essential pharmaceutical services, particularly in

Michael Page  10時間前
Michael Page 求人

Be part of a top 10 Global CRO thats entering the Japan market as a first member. Lead in RA activities to submit clinical trial documents to obtain approval. Client Details * Top 10 global CRO

Michael Page  10時間前

Overall The Manager of Government Affairs & Policy, Japan will be responsible for effective internal and external interactions to position J&J as a credible stakeholder to the local government and shape policies of strategic importance to

Johnson And Johnson  10時間前

RESPONSIBILITIES/PRINCIPAL DUTIES: The Senior Manager, Employee Engagement & Executive Communications, Janssen Japan is a leadership role in our Japan Pharmaceutical Communication & Public Affairs (CPA) team responsible for driving the engagement of our 1,000 employees in Japan

Johnson And Johnson  10時間前
Merck Group 求人

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich

Merck Group  2日前
CVS Health 求人

■ 職務内容 / Job Description Medical Communication Scientist (MCS) is a role name in AZKK and is generally known as medical writer. MCS is responsible for the authoring of clinical-regulatory documents and submission packages that communicate

CVS Health  6日前
BeiGene 求人

BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our

BeiGene  6日前

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