Jobs list of 6 - 16 million yen
-
Job number: JN -072024-11909 Posted: 2025-05-01
バイオ医薬品原薬プロセス開発研究者（産生株構築研究）
人々の健康や社会の発展に大きく貢献！6 - 10 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- We are engaged in the research, development, manufacturing, and sale of pharmaceuticals. We strive to maintain independent management, research, development, production, and sales functions, along with our unique international expansion efforts and the strengthening of our research and development capabilities. Focusing on strategic areas such as "cancer," we are accelerating the creation of promising new drugs, including antibody drugs. We also actively pursue global expansion, aiming to provide high-quality pharmaceuticals and services to patients worldwide.
- Responsibilities
- バイオ医薬品原薬プロセス開発研究者として、産生株構築研究に関わる下記業務をお任せいたします。
■業務内容：
◇バイオ医薬品の原薬製法開発および開発テーマ推進業務（抗体医薬品および新しいモダリティによる医薬品）
◇原薬製法に関わる新規技術開発および戦略立案（協力会社を含めた国内外企業等との共同研究業務を含む）
◇治験・承認申請における最新のグローバル規制要件を満たす試験デザイン立案、データ取得・ドキュメント作成
◇スケールアップ研究および国内外製造サイト技術部門への技術移管
■職務の魅力：
最先端の科学をベースにした革新的な製薬技術の開発とその技術を製品に反映することに注力しており、人々の健康や社会の発展に大きく貢献することができます。
国内外のステークホルダーとのコラボレーションなど、世界に向けた活躍の機会があります。
新薬候補物質の初期開発から上市に至るまでの医薬品開発ライフサイクル全般に関わることができ、当職種内でのキャリア形成と共に、適性に応じて、CMC開発全体のプロジェクト推進業務やサプライチェーンマネジメント業務、生産技術研究業務など、同社グループ内の多様なキャリアの機会があり、実際に多くのメンバーが幅広く活躍しています。
Patrick Chang
Industrial & Life Science -
Job number: JN -072024-11911 Posted: 2025-05-01
バイオ医薬品原薬プロセス開発研究者（培養プロセス研究）
人々の健康や社会の発展に大きく貢献！6 - 10 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- We are engaged in the research, development, manufacturing, and sale of pharmaceuticals. We strive to maintain independent management, research, development, production, and sales functions, along with our unique international expansion efforts and the strengthening of our research and development capabilities. Focusing on strategic areas such as "cancer," we are accelerating the creation of promising new drugs, including antibody drugs. We also actively pursue global expansion, aiming to provide high-quality pharmaceuticals and services to patients worldwide.
- Responsibilities
- バイオ医薬品原薬プロセス開発研究者として、産生株構築研究に関わる下記業務をお任せいたします。
■業務内容：
◇バイオ医薬品の原薬製法開発および開発テーマ推進業務（抗体医薬品および新しいモダリティによる医薬品）
◇原薬製法に関わる新規技術開発および戦略立案（協力会社を含めた国内外企業等との共同研究業務を含む）
◇治験・承認申請における最新のグローバル規制要件を満たす試験デザイン立案、データ取得・ドキュメント作成
◇スケールアップ研究および国内外製造サイト技術部門への技術移管
■職務の魅力：
最先端の科学をベースにした革新的な製薬技術の開発とその技術を製品に反映することに注力しており、人々の健康や社会の発展に大きく貢献することができます。
国内外のステークホルダーとのコラボレーションなど、世界に向けた活躍の機会があります。
新薬候補物質の初期開発から上市に至るまでの医薬品開発ライフサイクル全般に関わることができ、当職種内でのキャリア形成と共に、適性に応じて、CMC開発全体のプロジェクト推進業務やサプライチェーンマネジメント業務、生産技術研究業務など、同社グループ内の多様なキャリアの機会があり、実際に多くのメンバーが幅広く活躍しています。
Patrick Chang
Industrial & Life Science -
Job number: JN -072024-28343 Posted: 2025-05-01
サステナビリティ経営コンサルタント
◆異業界多数活躍/リモート環境有◆6.1 - 9.5 million yen Tokyo Consulting M&A Advisory / Strategy
- Company overview
- We are a global audit firm that originated as Japan\'s first nationwide audit corporation. With the slogan "Quality first," our professionals in audit and assurance services, as well as risk advisory, leverage their respective strengths to deliver valuable services. By combining the strengths of audit and assurance services with risk advisory, we contribute to enhancing corporate value and the development of capital markets. Our mission is to continuously capture and respond to evolving expectations through dialogue with diverse stakeholders.
- Responsibilities
- ■業務内容：
ESG投資が注目されている近年、そうした持続可能な社会づくりに向けた資金の流れについて、リスクアドバイザリーを行っていただきます。
<サステナブル経営高度化関連アドバイザリー業務>
パーパス経営、ビジョン、サステナブル方針策定支援
サステナビリティ戦略、マテリアリティ特定、KGI、KPI策定支援
サステナビリティインパクト可視化・経営管理統合支援（VBA、IWA、SROI等含む）
責任あるサプライチェーン構築・マネジメント（CSR調達方針策定、リスク評価等）支援
サステナブルマーケティング（エシカル消費含む）支援
ESGデューデリジェンス
ESGデータドリブン経営支援
<非財務情報開示関連アドバイザリー業務>
CSRD、SEC等の非財務情報開示の対応支援
統合報告書、サステナビリティ報告書等の作成支援
ESG評価（FTSE、MSIC、DJSI、CDP等）向上支援
<環境・社会課題ソルーション関連のアドバイザリー業務>
カーボンニュートラル施策実行支援（シナリオ分析、カーボンフットプリント算定、CO２排出量算定・削減・実装、SBT目標設定、TCFD対応、インターナル・カーボンプライシング、事業ポートフォリオ見直し等）
生物多様性マネジメント（現状調査、方針策定、戦略策定、TNFD対応支援等）支援
水リスクマネジメント（現状調査、方針策定、戦略策定等）支援
人権デューデリジェンス
人的資本経営構築支援
<サステナブルファイナンス関連アドバイザリー業務>
ESG投融資方針（PRI/PRB/PSI含む）支援
投融資先ポートフォリオ スコープ3排出量計測支援（PCAF対応、ファイナンスドエミッション算定）
投融資先とのエンゲージメント支援
インパクトファイナンス関連支援"
Yuhi Samejima
Consulting -
Job number: JN -072024-33628 Posted: 2025-05-01
タンパク質科学・質量分析分野の専門性を有する研究員
分子レベルでの相互作用解析手法の構築を伴う業務の経験を3年以上程度お持ちの方必見です。7 - 13 million yen Kanagawa Pharmaceutical Research & Development
- Company overview
- We are engaged in the research, development, manufacturing, and sale of pharmaceuticals. We strive to maintain independent management, research, development, production, and sales functions, along with our unique international expansion efforts and the strengthening of our research and development capabilities. Focusing on strategic areas such as "cancer," we are accelerating the creation of promising new drugs, including antibody drugs. We also actively pursue global expansion, aiming to provide high-quality pharmaceuticals and services to patients worldwide.
- Responsibilities
- タンパク質科学や分子間相互作用解析の専門性を通じた創薬/技術プロジェクトの推進業務をお任せ致します。
Patrick Chang
Industrial & Life Science -
Job number: JN -072024-38408 Posted: 2025-05-01
シニアDXプロジェクトマネージャー
グローバル展開を見据えた国内大手小売り企業でのPMポジションです。6 - 12 million yen Tokyo Information Technology IT Management
- Company overview
- Our client operates digital transformation business.
- Responsibilities
- システムの企画段階からビジネスサイドと並走し、さまざまな経営課題に対するソリューション提案をしていただきます。
商品企画、生産、物流、販売と広範なバリューチェーンに対するDXプロジェクトの企画設計から開発・保守運用全ての業務に携わっていただきます。
Yukiko Nakamura
Online / Inhouse -
Job number: JN -072024-38438 Posted: 2025-05-01
Business Associate
大手グループ内における新規事業開発8 - 13 million yen Tokyo Consulting Strategy Consultant
- Company overview
- Our client is a promotion of new business creation and open innovation.
- Responsibilities
- これまでグループが取り組んでこなかった領域や大きく成長が期待される領域への事業展開を進めております。
業務内容：
今後は、これまでの事業創出方法に加え、新たな領域の事業を R＆D（研究開発） をしていくという手法を用いて新規事業を創出していきます。
本ポジションでは、まさにイントレプレナーとして新しい領域への挑戦を推進していただく旗振り役を募集しております！
Yuhi Samejima
Consulting -
Job number: JN -072024-143827 Posted: 2025-05-01
品質保証 QA
Global Company6 - 12 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control
- Company overview
- We are engaged in the research, development, manufacturing, and sale of pharmaceuticals. We strive to maintain independent management, research, development, production, and sales functions, along with our unique international expansion efforts and the strengthening of our research and development capabilities. Focusing on strategic areas such as "cancer," we are accelerating the creation of promising new drugs, including antibody drugs. We also actively pursue global expansion, aiming to provide high-quality pharmaceuticals and services to patients worldwide.
- Responsibilities
- 医療機器、再生医療製品等を含む新たなモダリティへの業務展開
新たな技術の導入、技術の進化
サプライチェーンの多様化
グローバル製品（開発品・市販品）の増加
製造委託先、試験委託先ならびに原材料供給業者の増加
そのため、GQP/GMP/QMS/GCTP/GDP等に関する品質保証業務に精通した要員の補充が必要となった。
IND/IMPD、NDA/BLA作成及び推進、国内申請資料作成及び推進、その他CMC薬事にかかわる業務
Patrick Chang
Industrial & Life Science -
Job number: JN -072024-144988 Posted: 2025-05-01
【御殿場】バイオロジクス創薬推進における分析研究者
グローバルカンパニー！6 - 10 million yen Shizuoka Pharmaceutical Research & Development
- Company overview
- We are engaged in the research, development, manufacturing, and sale of pharmaceuticals. We strive to maintain independent management, research, development, production, and sales functions, along with our unique international expansion efforts and the strengthening of our research and development capabilities. Focusing on strategic areas such as "cancer," we are accelerating the creation of promising new drugs, including antibody drugs. We also actively pursue global expansion, aiming to provide high-quality pharmaceuticals and services to patients worldwide.
- Responsibilities
- 新規バイオロジクス開発や新規創薬技術開発におけるタンパク質分析ならびに新規分析技術の確立
Patrick Chang
Industrial & Life Science -
Job number: JN -072024-145099 Posted: 2025-05-01
[Tokyo/Shizuoka/Ibaraki] QA for Drug Development and New Product Launch
Rich Pipeline and Global Culture7 - 12 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control
- Company overview
- We are a leading pharmaceutical company in Japan, offering a wide range of products in the medical field. Our product lineup includes various pharmaceuticals to support patient health, and we are also dedicated to research and development. We strive to develop new treatment methods and medications to contribute to the treatment and prevention of diseases. Additionally, we operate globally, providing our products to patients worldwide. We uphold high standards of quality and safety, contributing to the advancement of healthcare and the well-being of patients.
- Responsibilities
- Contribute to development projects by ensuring the quality of investigational drugs used in clinical trials conducted globally and complying with regulations such as GMP.
Promotion of quality assurance operations such as management of investigational drugs, investigational drug substances and new product manufacturing contractors, change management in the development phase, implementation of quality audits, shipment of investigational drugs by appropriate product quality management, etc.
Building and collaborating with joint development partners
Improvement of global quality assurance system for developed products, continuous improvement, promotion of new regulation compliance
Promote regulatory inspection response and inspection preparation in cooperation with related departments such as laboratories, manufacturing contractors, and supply chains so that early application and launch of new products can meet and respond to regulatory requirements globally.
Participate in the global working team within Quality Assurance and Quality Technology to solve quality assurance issues and improve and improve the quality assurance system.
Initial development phase Quality assurance work at product manufacturing plants such as regenerative medicine
Martin Tsvetkov
Industrial & Life Science -
Job number: JN -072024-141505 Posted: 2025-05-01
Analyst
Analyst6 - 10 million yen Tokyo Pharmaceutical Market Access / Pricing / HEOR
- Company overview
- This is the exclusive business partner and adviser to biopharma senior management teams
- Responsibilities
- Demonstrated ability to be an important contact for the client in all communications
Ability to present independently to the client
Demonstrates strong understanding of assets that best fit the client
Ability to interact with partners and manage diligence requests
Able to trouble shoot assessment to evaluate target niches
Basic understanding of financial analysis and modelling, including DCF models and comparable transactions
Ability to author thought leadership pieces
Provide support in quality control and in ensuring the product is polished for Associate review
Having experience and understanding of the health care industry
Martin Tsvetkov
Industrial & Life Science -
Job number: JN -072024-167442 Posted: 2025-05-01
Partner Specialist (SDR)
Global working environment/Cloud technology6 - 8 million yen Tokyo Information Technology IT Sales / Business Development
- Company overview
- We are a global IT services and consulting company that supports business transformation through digital, technology, and consulting services. We provide digital strategy, IT consulting, systems integration, and outsourcing services, aiming to drive industry innovation and efficiency. Additionally, we leverage our global network and advanced technologies to deliver optimal solutions to our clients.
- Responsibilities
- The Partner Advisor is a dedicated point of contact for cloud partners, guiding them through all stages of business development to build and grow their cloud business and provide the best experiences for end customers. The core responsibilities include:Sales and Upselling:Conduct inbound and outbound product/service sales and upselling.
Execute daily outbound phone calls/emails, contact decision makers, build quick rapport, and assess needs.
Explain technical products/solutions and value propositions to businesses across various verticals and sizes, detailing how they address client needs.
Execute outbound prospecting campaigns to source, contact, and engage prospective customers interested in evaluating products.
Develop and lead outbound campaigns from idea generation through to initial pitch and pipeline qualification.
Lead and contribute to team projects to develop and refine the sales process.
Develop and codify best practices and sales workflows for interactions with prospects.
Achieve or exceed monthly sales quotas.
Reach out to existing customers to pitch new ancillary products or increase spending on currently used products.
Troubleshoot small technical setup issues or route them to relevant teams.
Renewals (Cloud):Manage the customer renewal sales process, identifying up-sell and cross-sell opportunities within accounts, and closing these agreements before contract expiration.
Educate customers on digital products.
Participate in the design, development, and implementation of programs to increase cloud renewals business.
Analyze data trends, market dynamics, and customer performance, identify opportunities, and create implementation plans to maximize results.
Support regional leads and partner community with training, materials, and ongoing support.
Engage and coordinate internal groups as needed to resolve customer issues and maximize customer retention.
Increase the number of upgrade executions.
React to client business needs and adapt internal procedures to provide services.
Manage daily renewal opportunities in the CRM system.
Work with account managers to provide clarity around executing upgrades.
Dejiddolgor Suuri
Tech Services -
Job number: JN -072024-4437 Posted: 2025-05-01
Japan Risk Management Leader
Rich pipeline, both Clinical and PMS9 - 14 million yen Tokyo Pharmaceutical Pharmacovigilance
- Company overview
- Our client is a leading global pharmaceutical firm with a presence in about 150 countries and a workforce of around 40,000 employees. The company is dedicated to advancing healthcare through innovative treatments across various therapeutic areas.
In Japan, the firm employs over 2,500 professionals focused on delivering solutions tailored to the specific needs of the local population. By integrating global advancements with local insights, the company collaborates closely with healthcare providers to ensure effective and accessible therapies.
Committed to sustainability and corporate responsibility, the firm strives to improve patient outcomes and enhance the quality of life. Its efforts make significant contributions to both the local and global healthcare landscape. - Responsibilities
- ake full accountability to create, implement and verify J-RMP activities including EPPV, risk communication activities and aggregate reporting such as J-DSUR, J-PSUR, Periodic Infection Report and Non-serious unlisted periodic report including reports for medical devices and all activities related to Post-Marketing Surveillance/Clinical study/Database research.
Take full accountability to prepare Re-examination dossier and GPSP compliance inspection in responsible products/compounds.
Lead and manage PvA and PMSO in responsible products/compounds.
Lead and facilitate J-SMT meeting in collaboration with JPKK’s key stakeholders including JCoT members.
As an extended member of Global Safety Management Team(G-SMT), liaise with G-SMT of responsible products/compounds.Join JCoT, NPI and other related committee with license partner companies as a representative for J-SMT of responsible products/compounds and proactively lead safety risk management related discussions and take necessary actions by covering early stage of clinical development though postmarketed phase of products.
Lead and contribute to the prevention and rapid resolution of local safety risk management related issues including timely stake holder management (internal and external) of responsible products/compounds.
Plan and monitor budgets and controls expenditures for responsible products/compounds in collaboration with Group manager/ Director.
Contribute to the implementation of continuous process improvements from advanced safety management point of view by utilizing latest technologyes while enhance sustainable efficiency in collaboration wih SPMD.
Understand the rule and principle of the relevant regulations such as PMD Act., GCP, GVP and GPSP and ensure compliance to those regulations, within own responsibility.
Patrick Chang
Industrial & Life Science -
Job number: JN -072024-9212 Posted: 2025-05-01
【茨城・筑波】薬理受託試験サービスマネージャー（オンコロジー領域）
ピープルマネジメント経験が生かせます8 - 11 million yen Ibaraki Pharmaceutical Research & Development
- Company overview
- We produce a variety of mice and rats, and also provide feed and bedding. This allows researchers to focus on animal care, management, and research. Additionally, we collaborate with the United States to conduct virus testing on animal cells and provide contract manufacturing of monoclonal antibodies. Our fundamental principle is to produce and supply experimental animals based on scientific knowledge, supporting the development of life sciences by ensuring a stable supply of high-quality experimental animals that become the global standard.
- Responsibilities
- ・Oncology領域受託試験サービスの業務管理・予算達成
・PDX（Patient-Derived Xenograft）/ Immuno-Oncology事業の拡大戦略策定 / 実行
・受託試験サービスにおける顧客対応
・従業員管理
Patrick Chang
Industrial & Life Science -
Job number: JN -072024-35827 Posted: 2025-05-01
HR
ベンチャー企業でのHR6 - 8 million yen Tokyo Human Resources HR Generalist
- Company overview
- We provide a platform that enables the rapid construction of business systems, empowering many individuals to become product creators. This platform offers highly flexible and scalable core systems for large and medium-sized enterprises.
In recent years, as the trend of combining cloud SaaS specialized for specific use cases accelerates, we are pioneering the construction of next-generation business application platforms. In the Japanese market, where outsourcing to system development companies is common, we provide backend and frontend application development and business consulting on our own platform.
By leveraging the latest technology and creativity, we aim to support the future society by solving corporate management challenges. - Responsibilities
- 採用・評価制度・人材開発を中心に組織を一緒に創ってくださる方を募集します。事業を成長に導くための「人」と「組織」にまつわる戦略策定と実行を実現していただきます。 業務内容：
事業計画の実現のための組織設計
採用戦略の立案と実行
評価制度の設計、継続的なアップデート
オンボーディング、人材開発の企画立案・実施
Misato Nakao
Corporate Services -
Job number: JN -072024-141975 Posted: 2025-05-01
Digital Marketing Project Manager
Digital PM12 - 16 million yen Tokyo Pharmaceutical Marketing
- Company overview
- We are a foreign pharmaceutical company. Through a merger with an international biopharmaceutical company, we have introduced innovative biotechnology to the Japanese market. Through highly specialized medical information activities, we are enhancing our presence in the Japanese market. Focusing on cancer, cancer immunotherapy, and infertility treatment, we provide innovative healthcare solutions to the people of Japan.
- Responsibilities
- Manage eCommerce and/ or other digital projects
Lead and manage related projects. Interact with internal and overseas stakeholders.
Plan eCommerce and Digital strategies
Support Head of eCommerce & Digital to devise eCommerce and Digital strategies. Discuss with internal (domestic/ overseas) stakeholders, promote initiatives, and concretize initiative details and ROI.
Responsible for leading/ managing related projects. Interact with internal and overseas stakeholders.
Martin Tsvetkov
Industrial & Life Science -
Job number: JN -072024-142337 Posted: 2025-05-01
メディカルアフェアーズ本部 肺高血圧症疾患領域スペシャリスト
メディカルアフェアーズ本部 肺高血圧症疾患領域スペシャリスト6 - 10 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is a leading global pharmaceutical firm with a presence in about 150 countries and a workforce of around 40,000 employees. The company is dedicated to advancing healthcare through innovative treatments across various therapeutic areas.
In Japan, the firm employs over 2,500 professionals focused on delivering solutions tailored to the specific needs of the local population. By integrating global advancements with local insights, the company collaborates closely with healthcare providers to ensure effective and accessible therapies.
Committed to sustainability and corporate responsibility, the firm strives to improve patient outcomes and enhance the quality of life. Its efforts make significant contributions to both the local and global healthcare landscape. - Responsibilities
- Responsible to develop the Medical Affairs product strategy through the analysis of medical needs collected from all internal & external stakeholders of the therapeutic area
Responsible for managing MAF study / publication portfolio in alignment with brand strategy
Responsible for people and operational budget management of PH (Pulmonary Hypertension) therapeutic area
Day to day project management for activities based on the Medical Affairs Plan in responsible disease areas
Responsible for ensuring that all Medical Affairs activities are compliant with Japan Legislation and HCC (Healthcare Compliance) rules.
Patrick Chang
Industrial & Life Science -
Job number: JN -072024-142574 Posted: 2025-05-01
Regulatory Strategist
RA8 - 12 million yen Tokyo Pharmaceutical Regulatory Affairs
- Company overview
- Our client is one of the most well-established European-based international pharmaceutical companies in Japan.
- Responsibilities
- Build a registration strategy for efficient product development in Japan to get fast approval of new projects (new product, new indication, new dose & administration, new formulation, etc.).
Coordinate the relevant functions to prepare the documents which should be submitted to PMDA and/or MHLW such as the documents relevant to PMDA consultation and Orphan Drug Designation.
Support the dossier manager to lead the relevant functions to prepare the required documents for NDA/sNDA submission and answer documents to inquiries during NDA/sNDA review by PMDA, and conduct the following activities.
Ensure other functions to prepare the documents to be submitted to Health Authority on products.
Contribute to the global regulatory activities on projects in charge by inputting regulatory strategy in the global regulatory strategy.
Provide Global Regulatory Team (GRT) with the Japanese legal/regulatory requirements and Japanese development strategies if necessary.Graps the regulatory information such as HA’s movement, legal requirement on NDA/sNDA guidelines, etc
Martin Tsvetkov
Industrial & Life Science -
Job number: JN -072024-146307 Posted: 2025-05-01
【東京】臨床開発プロジェクトマネージャー
臨床開発プロジェクトマネージャー経験者必見です!6 - 9 million yen Tokyo Pharmaceutical Clinical Development
- Company overview
- We are committed to providing high-quality products and delivering appropriate safety information to patients and consumers worldwide. In our pharmaceutical business, we focus on developing anticancer drugs and other medications, offering treatments for cancer, immunology, allergies, and urology. Additionally, in our consumer healthcare business, we cultivate well-loved brands that contribute to the health and well-being of consumers over the long term.
- Responsibilities
- 臨床開発プロジェクトのスケジュール・リソース・コスト管理
社内意思決定プロセス管理
関連部門（臨床開発、薬事、非臨床、CMC等）で構成されるプロジェクトチームのコミュニケーションマネジメント
共同開発先・導出入先との協業プロジェクトのアライアンス業務
歓迎条件:
海外スタッフを含むグローバルチームでの業務経験
上級レベルの英語コミュニケーション能力 （グローバルチーム会議をファシリテートできる会話能力）※海外拠点や海外他社協業先とのグローバルプロジェクトの担当機会あり
抗がん剤領域の新薬開発経験
プロジェクトマネジメント管理ソフトの使用経験（例：MS-Project、Planisware等）
Project Management Professional （PMP）資格
Patrick Chang
Industrial & Life Science -
Job number: JN -072024-137932 Posted: 2025-05-01
MD
2nd in MD to be hired in JP12 - 15 million yen Tokyo Pharmaceutical Medical Doctor
- Company overview
- We are engaged in the research, development and provision of medical technologies in Japan. In particular, we focus on the development of innovative therapies and provide advanced technologies related to cancer treatment. We use a new therapeutic approach called photoimmunotherapy to target cancer cells for effective treatment. This technology combines light and drugs to selectively destroy cancer cells. In research and development, we are strengthening our collaboration with specialized institutions and universities in Japan and overseas to conduct clinical trials and commercialize the technology. We are committed to innovation in the medical field and to improving the quality of life of patients.
- Responsibilities
- Collaborate with Cross functional members to contribute to the development of products desired in the medical field and to maximize of product value.
Participate in discussions on optimizing our technology with algorithms.
Understanding of our treatments through discussions with KOLs at our target hospitals.
Support sales from science perspective as the core of medical communication that emphasizes compliance.
Join the discussion with KOLs for proper use of Illuminox to meet “Unmet Needs” in cancer treatment.
Conduct a wide range of medical / science activities such as doctor-led clinical trials, publications, and advisory board meetings.
Evaluation and support of clinical trials, presentations at academic conferences on clinical trials, publications, promotional materials, web contents, information on briefing sessions, etc. Manage operational aspects of clinical trials from study start-up through database lock as assigned, with adherence to stated goals, timelines, budgets, and applicable regulatory requirements.
Martin Tsvetkov
Industrial & Life Science -
Job number: JN -072024-142387 Posted: 2025-05-01
[Daiichi Sankyo] プロジェクトマネジメント
CROで開発業務5年以上かつプロジェクトマネジメント業務の経験をお持ちの方必見で7 - 10 million yen Tokyo Pharmaceutical Clinical Development
- Company overview
- Our client a major Japanese pharmaceutical company engaged in the research, development, manufacturing, and sales of pharmaceuticals. Our group promotes four business areas—new drugs, generics, vaccines, and OTC products—to meet diverse medical needs. By expanding our operations globally, we aim to provide innovative treatments to a wide range of patients. Additionally, we possess advanced technological capabilities and well-equipped facilities to support our research and development. We actively conduct clinical trials both domestically and internationally, striving to demonstrate leadership in the pharmaceutical industry while emphasizing our commitment to contributing to society as a whole.
- Responsibilities
- 開発プロジェクトにおけるプロジェクトマネジメントとして、グローバルプロジェクトチームのマネジメント、開発戦略計画、予算、タイムラインおよび課題管理・解決をお任せいたします。
Patrick Chang
Industrial & Life Science