Jobs list of Pharmaceutical & Medical Affairs
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Job number: Job-00232759 Posted: 2023-06-15
【神奈川／東京】グローバル開発薬事
5年以上のR＆Dにおける薬事経験が活かせます。15 - 18 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is conducting research and development in regenerative medicine.
- Responsibilities
- 心筋細胞、膵島細胞の両開発資産に対するグローバル規制戦略の策定をリードする
ビジネスユニットヘッドをサポートし、グローバルの申請データパッケージの設計を行う
FDAなど海外の規制当局と協議する際のリエゾンとして、IND申請に必要なCMCデータパッケージや前臨床データパッケージの適切性、薬事申請をサポートする試験デザインなど、あらゆるトピックについて責任を担う
Presidentと直接連携し、投資家、株主、キーオピニオンリーダー、メディアなど、グローバルな主要ステークホルダーとの間で加速の可能性を含むあらゆる規制関連事項を提示し、議論する
会社のビジョン・ミッション・目的を達成するために、全社的なタスクをリード・参加する
Patrick Chang
Pharma -
Job number: Job-00203428 Posted: 2023-06-15
Medical Manager
Strategy planning and data gathering13 - 17 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- This company is one of the world’s leading pharmaceutical companies.
- Responsibilities
- STRATEGY:
Act as Local Medical Affairs TA expert in one or more TAs
Support the Brand or launch teams/ Local TA leadership team in the development of TA, Launch and Brand strategies
Lead Medical Affairs activities in assigned territory along defined local Medical Launch / Brand strategies
Consolidate and communicate trends, market insights, and unmet needs identified in the field
OPERATIONS:
Develop Medical material, review marketing material, trainings
Ensure scientific and clinical accuracy for specific product or brand
Receives adverse event reports and transmits such reports internally according to Company procedures
Ensures timely completion and up-to-date knowledge of Company policies / SOPs, and local laws and regulations
Maintains up-to-date GxP knowledge by following internal and external trainings
Conduct Local internal scientific training and ensure continuous Medical education of existing teams and new employees working in the Local TA
Develop Medical KTL development plans
Positively impact external perceptions and knowledge regarding company and company products
Maintain and demonstrate comprehensive and in-depth scientific TA knowledge when executing assigned tactics
Ensure operational excellence by sharing best practices
Map treatment landscape and medical environment for new indications/ programs
Provide support in the planning and tracking of the (TA-specific) medical budget
DATA GENERATION AND DISSEMINATION:
Lead/ support (depending on nature of study) Medical studies, assist to coordinate Local clinical projects and contribute to site selection for clinical projects
Lead Local publication process, publication dissemination and alignment with Local, Regional and Global publication plan
Act as a resource, liaison and facilitator for ISS and investigators that are aligned to the Medical Affairs strategy
Coordinate with ClinDev and ClinOps in providing field support for research studies and assist in the selection of clinical study sites
Assimilate, process and share medical information with stakeholders
STAKEHOLDER ENGAGEMENT:
Provide training to HCPs and support in realising Medical educational events
Interact with Local stakeholders in Medical community in TA
Identify and interact with influential members of the Medical community (HCPs/external experts) and other healthcare stakeholders (managed care organisations, government organisations, patient groups) within assigned territory and TA
Represent company at Medical Education events, programs, meetings and support patient advocacy related activities
Partner with external stakeholders to develop innovative solutions
Engage with internal colleagues (Medical Affairs department, Clinical Operations, Commercial colleagues as appropriate, etc.) in developing and delivering and participating in Medical or cross-functional initiatives
Martin Tsvetkov
Pharma -
Job number: Job-00266093 Posted: 2024-04-09
Specialty Care Medical Affairs Lead
Medical Affairs Lead position at global mega-pharma12 - 22 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- This company is the world\'s leading pharmaceutical company.
- Responsibilities
- Leadership of medical team, including setting business objectives, performance management and team development
Responsibility for development of the Medical Plan/Strategy for relevant therapeutic areas
Recruitment, development and retention of talented colleagues as well as coaching and guidance of colleagues to support them achieving their maximal potential
Membership of Medical and Commercial Leadership Teams
Resource allocation to ensure appropriate resources to fulfil medical objectives and business needs
Ensure compliance of medical team with country Code of Practice and relevant SOPs, regulations and guidelines
Collaboration with internal stakeholders to ensure timely receipt of information on brand strategy, clinical plan, new clinical data, new regulatory and safety information and accurate, balanced and up to date materials to use in medical to medical communications
Work with key external stakeholders during the life-cycle of the company's medicines, supporting the company strategy and bringing external insights to the organization to shape strategy and providing focused, relevant information in response to their needs
Review and certification of promotional and non-promotional materials and activities and approval of customer engagement programs
Ensure that product materials and related activities reflect the most up to date regulatory labelling and risk management plans and regulatory commitments
Input into regulatory submissions, clinical overviews, license variations and CDS updates as required
Input into HEOR submissions, HTA dossiers, clinical guideline consultations and regional formularies as required
Input into assessment and due diligence of business development initiatives
Support for issues related to supply and distribution, product quality, benefit-risk, market actions and product withdrawals related to portfolio
Support for in country clinical research programs, including protocol and site feasibilities related to portfolio
Protocol approval and oversight of in country non-interventional studies related to portfolio
Support for investigator initiated research (IIR) studies to ensure that appropriate records are kept and progress is monitored
Support for media, government and patient group activities, including policy development, corporate initiatives and issues management
Participate in local, regional and global cross-functional project teams to ensure that ongoing improvements in processes and performance are delivered
Accountable for medical team IIR and headcount/expenses budgets
Represent the country and countries interests to European and Global teams
Yui Osone
Pharma -
Job number: Job-00264262 Posted: 2024-02-26
メディカルフェアーズ部長候補
製薬会社でのメディカルアフェアーズ経験3年以上お持ちの方必見です。10 - 12 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is a pharmaceutical company.
- Responsibilities
- 製品メディカル戦略、年度方針の立案
KOL対策並びに学会対策
製品および疾患に関連する情報収集、情報発信
メディカルアフェアーズ、メディカルサイエンスリエゾンとしての対外対応
市販後製品に関するパブリケーション、ライフサイクルマネジメント
新薬上市準備に関する対外対応
関係部署に対するメディカルサポート
Patrick Chang
Pharma -
Job number: Job-00267036 Posted: 2024-04-11
メディカルサイエンス職
研究およびメディカル活動を計画、実行する経験が活かせます。10 - 13 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is a biopharmaceutical company.
- Responsibilities
- 領域における最新情報やアンメットメディカルニーズ等の情報を収集・分析することで、メディカルギャップを特定し、患者さんに貢献するためのメディカル戦略を計画、実行する。
Patrick Chang
Pharma -
Job number: Job-00262783 Posted: 2024-01-31
Senior Manager, Scientific Writing
薬事申請書類作成経験、または同等の資格・経験が活かせます。9 - 14 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Out client is a global company dealing with pharmaceutical products.
- Responsibilities
- DTから提供される情報をもとに、薬事申請書類作成方針のストーリーボードを構築し、グローバルチームとすり合わせを行い、状況に応じた執筆戦略の観点からチャレンジングな提案を行う。
DOCリードとして、グローバルなオーサリング薬事申請書戦略を理解し、臨床品目の国内薬事申請書のファイナライズをリードする。
オーサリング完了までの適切かつ最短のスケジュールを設定し、それを遵守する。また、状況に応じてプロセスの観点からチャレンジングな提案を行い、目標スケジュールの短縮を図る。
PMDAの審査報告内容や照会事項に関する各審査部門の傾向を踏まえ、最適な申請資料作成戦略をチームに提案し、プロセス改善をリードする。
ストーリーボードに基づき、J-CDL／J-CSで臨床モジュールを完成させる。
必要に応じてグローバル申請資料を管理し、関係者に提供する。
CSRオーサーとしてオーサリング、調整活動を行う。
検査におけるCSRオーサリング部分を担当する。
外注ベンダーを戦略的に活用した業務遂行を管理し、成果物の品質を確保する。社内外のプロセスやガイドラインを遵守する。
必要に応じて他の臨床／規制文書をレビューし、編集する。
プロセスの特定と簡素化により、継続的なプロセス改善を推進する。収集したメトリクスからの情報に基づいて、部門横断的なビジネスプロセスの改善をリードする。
シニア・サイエンティフィック・ライターとして、他のサイエンティフィック・ライターが日本向けの臨床／薬事文書を作成する能力を向上できるよう助言を行う。また、経験の浅いJ-Docリーダーに指導とサポートを行う。
日本チームが本社のカウンターパートや臨床研究、薬事などの主要なステークホルダーと良好なコミュニケーションが取れるよう、社内外に協力的な職場環境を構築し、付加価値を提供する。
グローバル科学・規制文書（GSRD）
リーダーシップチームとの良好なコミュニケーションを図り、日本での申請におけるGSRDとの連携を促進する。
イレギュラーな申請や未経験の申請・相談に対しても、メディカルライティングの観点から社内メンバーにアドバイスを行う。
Patrick Chang
Pharma -
Job number: Job-00216925 Posted: 2023-06-15
RA/Mgr, Reg Affairs
薬事マネジャーあるいはそれに準ずる経験をお持ちの方必見！8.5 - 14 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is the largest provider of biopharmaceutical development and commercial outsourcing services.
- Responsibilities
- ■部門紹介：・マネジャーとしてICCC（治験国内管理人）試験の薬事担当者としての業務を行う部員をまとめ、組織の運営にあたります。・自身もICCC試験の薬事担当者としての業務を行います。｜治験国内管理人として、日本法人を有しない治験依頼者に代わり治験計画届を提出し、管理を行います。・規制に関する社内外の問い合わせに対して回答・アドバイスを行います。◇具体的には・薬事部員の教育、育成｜規制の解釈、疑問点に関する社内外の問合せに対して薬事としての判断、助言を提供。必要に応じて規制当局に確認・Project Teamに薬事担当者として参加し、薬事面のサポートを実施｜治験計画届書及び提出資料のレビューを行い、必要に応じて助言、修正・当局からの照会事項に対して、依頼者と協力して回答書を作成し提出
■業務内容：・治験依頼者に対する規制要件の説明｜治験計画届及び添付資料の内容確認｜治験計画届提出後などのPMDA対応・治験期間中に発生する問題に対する薬事対応｜規制要件に関する判断、助言｜信頼性調査対応・対面助言のサポート業務｜SOP等手順書の作成、レビュー
Patrick Chang
Pharma -
Job number: Job-00254746 Posted: 2023-09-07
【東京】開発薬事 マネジャー/担当部長 ～JASDAQ市場グロース上場～
製薬メーカーでのマネジャー～担当部長ポジションです8 - 15 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- The company is a pharmaceutical manufacturer that actively develops orphan drugs.
- Responsibilities
- ■職務概要：
がん、血液領域、ウイルス感染症を中心に希少疾患領域の開発を目指すJASDAQ市場グロースに上場の製薬企業の開発薬事マネジャー～担当部長ポジションです。
■職務内容： 国内の薬事関連法規・通達等の調査・検討、開発計画に対する薬事的戦略及び承認申請戦略の立案
治験計画届出、対面助言相談実施、製造販売業許可に必要な書類の作成・諸手続き
製造販売承認申請/一部変更承認申請のためのCTD資料作成及び承認申請関連の薬事関係書類の作成・諸手続き
添付付書の作成・諸手続き及び維持管理業務
薬価基準収載に係る申請資料作成・諸手続き
上記手続きに係る公官庁との連絡・折衝業務
各種プロモーション資材に対する作成支援業務
開発薬事業務に関係する手順書・マニュアルの作成・整備
Patrick Chang
Pharma -
Job number: Job-00210272 Posted: 2023-11-06
Medical Affairs PM
Medical PM8 - 14 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is a global healthcare corporation. Driven by its mission and aspirations, the organization is fully committed to safeguarding public health. This commitment is demonstrated through ongoing endeavors involving the research, development, importation, manufacturing, and distribution of medicines and vaccines. Its parent company is headquartered in the United States.
- Responsibilities
- 1) In research projects led by companies, manage research projects and contribute to the creation of evidence according to the plan.In the research project, as a member of the study team, in the process of planning, budget management, execution, and publication of results, internal related departments (R & D headquarters, legal / compliance department, purchasing department, finance department, etc.), the US headquarters, and outside the company Collaborate with partners.
In the research planning phase, develop a research timeline and budget plan, and lead the research feasibility assessment.
In the start preparation phase, we will be in charge of a wide range of tasks such as vendor selection, facility selection, various contract creation, and internal regulation assessment, and promote the project so that the research start can be achieved on timeline. In the execution phase, manage the project to proceed as planned through vendor management, cost management, and schedule management. We will also strive to ensure the quality of research.
Work to comply with compliance by conducting research based on ethical guidelines and various laws and regulations and guidelines while coordinating with related departments within the company.
For US headquarters-led research, work with headquarters personnel to promote the project.
2) In collaboration with researchers and their research institutes, the US headquarters, and related departments within the company (Medical Affairs, R & D Headquarters, Legal and Compliance Department, etc.), while maintaining the independence of researchers and the neutrality of research. Manage and execute researcher-led research (IIS) support operations and support the creation of innovative evidence by Japanese researchers.Responsible for researchers / research institutes and US headquarters in collaboration with related departments throughout the entire process of supporting IIS applications, contracting adopted projects, providing research funds and research drugs / compounds, preparing for research start, conducting research, and reporting results. Coordinate / negotiate with other parties and manage / execute IIS support operations.
In the field of cancer where research on new treatment methods is advancing, doctor-initiated clinical trials are also covered by the IIS support system, and if adopted by the examination, research funds and investigational drugs will be provided to provide future new cancer treatments. Support the development of law.
Collaborate / collaborate with related departments within the company to creatively find solutions when introducing an unprecedented new research support system.
Post the latest information on the IIS support system developed by the US headquarters worldwide on an external website, and provide detailed information on the system and procedures to researchers considering application in collaboration with related departments within the company. ..
When making a research contract with a research institution to which a researcher belongs, prepare a draft contract, negotiate a contract, and conclude a contract.
After starting the research, we will confirm the progress of the research (including the status of publication) based on the contract, arrange the provision of research drugs / compounds, and pay the research expenses according to the milestone.
Martin Tsvetkov
Pharma -
Job number: Job-00266310 Posted: 2024-03-29
ノンラインマネージャー
新薬登録を含むRA分野での5年以上の経験をお持ちの方必見です。8 - 11.5 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is a global pharmaceutical company.
- Responsibilities
- 内部インターフェース日本国内の各部門との情報交換および対話：規制問題、医療、法務、HP 供給およびマーケティング監督総局。
グローバル機能との情報交換と対話：グローバル規制問題、企業医療および資産チーム、グローバル品質。
外部インターフェース必要に応じて、保健当局、業界団体、ライセンスパートナーとの対話と交渉。
Martin Tsvetkov
Pharma -
Job number: Job-00222832 Posted: 2024-02-16
[Organon] Medical Advisor/MSL
MSL8 - 16 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is a global pharmaceutical company
- Responsibilities
- Scientific Leadership:
Communicate scientific therapy needs credibly, appropriately, and effectively across a variety of internal and external stakeholders at all levels.
Build trust with the external scientific community via peer-to-peer scientific exchange, research and educational collaborations, interactions with scientific societies and health organizations, publications, etc.
Provide therapeutic/functional training to assigned teams and affiliate functions.
Develop and help execute country medical educational programs and symposia.
Lead country Advisory Boards and Expert Input Forums in line with strategy.
Participate in and contribute significantly to professional organizations, academic or regulatory working teams.
Lead executes country medical educational programs and symposia.
Medical Strategy and Therapy Leadership:
Translate Global Medical Strategies into research, data analysis, scientific communication, educational, and other tactics and solutions that improve patient outcomes and enhance access in the country.
Ensure effective communication and collaboration between field and Medical through providing scientific and medical support to the Commercial team.
Evaluate accuracy of promotional materials.
Provide Medical Affairs therapeutic area support through engaging with SLs/KDMs, driving scientific initiatives and supporting the field force.
Collect, analyze, and communicate actionable insights at the country level.
Provide scientific inputs for digital initiatives.
Successfully collaborate, provide scientific inputs, and lead resolution of Regulatory queries/issues.
Support execution of and quickly adapt tactical plans to business realities in country.
Act with ethics and integrity; Provide non-promotional, balanced, reliable and scientific information.
Support with therapy training content for Sales team.
Demonstrate strategic thinking, specifically related to asset value proposition, and clinical and value evidence.
Support creation of Medical Affairs Plans along with the TA and Country Medical Leads.
Martin Tsvetkov
Pharma -
Job number: Job-00210945 Posted: 2024-01-21
R&D Japan/ Group Manager, Innovation Management Office
Alliance / Open Innovation8 - 16 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is developing and providing various medicines for an array of health concerns.
- Responsibilities
- All R&D communication physically such as THM and/or virtually such as via e-mail/R&D Portal site etc. R&D regular leadership communication such as RD SLT and LT.
Any R&D responsible technology-based innovation initiatives such as Robotic Process Automation, Cloud based cross functional team communication, as well as center of excellence to shard service provider at R&D. In addition to that the Group will provide service to lead non-R&D specific career development program to whole R&D, as well as to be responsible for new grads program execution.
Patrick Chang
Pharma -
Job number: Job-00266382 Posted: 2024-04-01
エビデンス創出・パブリケーション（リーダー候補～リーダー）
メディカルアフェアーズ部門での5年以上の職務経験をお持ちの方必見です。7.5 - 11.6 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is one of the leading pharmaceutical companies in Japan.
- Responsibilities
- 中枢神経領域、腎・糖尿病領域、自己免疫疾患領域の各種研究（臨床研究、医療データベース研究等）の計画立案および学会発表、論文投稿等のパブリケーション業務
Patrick Chang
Pharma -
Job number: Job-00239744 Posted: 2023-06-15
薬事機能リーダー
5年以上の薬事経験をお持ちの方必見です。7 - 11 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is a biopharmaceutical company.
- Responsibilities
- がん、神経、自己免疫等の各疾患領域や新規モダリティの製品開発において開発～市販後における薬事戦略の立案および当局折衝（PMDA/MHLW/FDA/EMA/China/Taiwan/Korea）を行う。
機能横断（CMC、非臨床、臨床、安全性）のメンバーで構成される申請・審査対応チームを統括し、国内申請・審査対応計画の立案・実行を行う。
パートナー他社のGlobal regulatory leader及び同社の海外子会社と連携、協働する。
Patrick Chang
Pharma -
NEWJob number: Job-00218125 Posted: 2024-04-18
Hematology MSL
Hematology MSL7 - 12 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is developing and providing various medicines for an array of health concerns.
- Responsibilities
- 血液疾患領域において自社のメディカルポジション(世評、信用)の確立。
自社製品並びに関連疾患領域に関する最新の医学・医科学情報を提供。
HCPから依頼があった場合に限り、未承認薬・適応外薬等に関する情報を提供。
メディカルアフェアーズプランで言及されるメディカル戦略に従い活動。
メディカルアフェアーズの疾患領域チームで合意したKOLリストを基に個々のKOLに対し計画を立て活動。
HCPとのコミュニケーションを通じてメディカルニーズの収集と評価を行い、インサイトの探索ならびにメディカルアフェアーズプランの策定および更新に貢献。
企業主導型臨床研究の実施支援、および医師主導型臨床研究関する助言・支援。
メディカルエデュケーションプログラムおよびアドバイザリーボードの実施支援。
医薬情報担当者への研修の支援。
Patrick Chang
Pharma -
Job number: Job-00252648 Posted: 2023-08-01
薬制薬事担者
製薬、医療機器業界における薬制・薬事業務の経験が活かせます。7 - 12 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is a biopharmaceutical company.
- Responsibilities
- 許可等業者の法令遵守体制の維持・管理（手順書作成・運用、会議体事務局、GQP/GVP部門との連携等）
国内および海外子会社における製品リスク（回収、偽造医薬品等）への対応
医薬品（再生医療等製品等新規モダリティ含む）及び医療機器の開発・上市に向けた薬事規制に関連する調査、社内連携のリード
社内における薬機法等の薬事規制に関する疑義照会対応業務
海外での医薬品販売承認維持のための薬制業務及びプロジェクトマネジメント業務
国内外の規制当局との授受文書の管理業務
国内及び海外当局等から発出される各種薬事規制の収集・分析・社内への適用推進業務
GMP/QMS/GCTP適合性調査（承認前調査/定期調査）、外国製造業者認定の維持・管理業務
製造委託先への製造・試験法に関する調査等（承認書と製造実態の整合性に係る年次点検、日局改正対応状況の確認等）
Patrick Chang
Pharma -
Job number: Job-00266339 Posted: 2024-04-05
Medical Science Liaison (MSL) - 自己免疫領域
MSL position at global maker with strong pipeline7 - 11 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is one of the top medicine and Clinical Research companies worldwide.
- Responsibilities
- 業務内容：
領域専門医等のリクエストに応じて、最新医学・科学情報を提供・議論する。
領域専門医等の意見、疑問、ニーズならびに共同研究などの機会を探索・収集し、社内関連部署と連携して解決策を探る。
サイエンティフックエキスパート(SE)との関係構築および維持をする。
メディカル部門主導イベント（アドバイザリーボード等）を社内医学専門家と協働して実施する。
Yui Osone
Pharma -
Job number: Job-00257467 Posted: 2023-10-26
【東京】開発薬事※マネージャー候補
薬事部門のマネジメント経験者必見です!7 - 12 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is providing drug development service.
- Responsibilities
- 部門の管理、人財マネジメント
営業活動
部門の予算管理
医薬品・医療機器関連の治験相談
メディカルライティング業務管理
医薬品・医療機器に関する法規制への対応業務
各国申請代理人との連絡・調整
当該国薬事規制等の調査
アジア地域における医薬品・医療機器開発戦略コンサルティング （各種試験成績・資料の評価、医薬品・医療機器承認申請に係る当局対応、申請届出等）
Patrick Chang
Pharma -
NEWJob number: Job-00264482 Posted: 2024-04-19
Medical Science Liaison (MSL) - 糖尿病領域
MSL position at global maker with strong pipeline7 - 11 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is one of the top medicine and Clinical Research companies worldwide.
- Responsibilities
- 職務内容/Job Responsibilities担当疾患領域（糖尿病／循環器疾患）の専門家として病態や治療薬に関する深い知識を背景に、領域専門医等からの医学・科学的な疑問点やニーズに対応することにより、患者さんの病状改善やＱＯＬ向上に貢献する。また領域専門医等との議論を通じて得た意見やニーズを社内関係部署に還元し、製品価値の最大化に貢献する。
主な職責/Primary responsibilities領域専門医等のリクエストに応じて、最新医学・科学情報を提供・議論する
領域専門医等の意見、疑問、ニーズならびに共同研究などの機会を探索・収集し、社内関連部署と連携して解決策を探る。
サイエンティフックエキスパート（SE）/ソートリーダー(TL)との関係構築並びに良好な関係維持を行う。
Yui Osone
Pharma -
Job number: Job-00213095 Posted: 2023-06-15
Medical Affairs Review Specialist
Medical review7 - 10 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is a global healthcare corporation. Driven by its mission and aspirations, the organization is fully committed to safeguarding public health. This commitment is demonstrated through ongoing endeavors involving the research, development, importation, manufacturing, and distribution of medicines and vaccines. Its parent company is headquartered in the United States.
- Responsibilities
- 資材・スライド等の検証
社内コンプライアンス研修
部門横断プロジェクトのリード
Martin Tsvetkov
Pharma
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