詳細条件から探す

大手内資製薬メーカーにて機械学習と生成AIの運用に特化したエンジニアを求めています。

仕事内容

（雇入れ直後）
・Act as an outstanding scientist of discovery ADME function.
・Responsible for the analysis, interpretation, integration and reporting of preclinical ADME data.
・As part of the integrated project teams, design and execute in vitro/in vivo studies to understand the relationship between pharmacokinetics (PK) and pharmacodynamics (PD).
・Clarify ADME profiles to optimize compounds based on their ADME profiles requirements, ensuring alignment with project timelines and regulatory standards.
・Interact/manage external vendors (CROs, academic sites etc.) for conducting in vivo and in vitro experiments.
・Align with overall Oncology Research strategy and objectives.
・Partner with other teams in Oncology Research as well as Development to translate scientific insights into actionable ADME/formulation strategies.

応募条件

【必須事項】

・Science degree MS, or exceptional experience in Pharmaceutical Sciences, Chemistry, Biochemistry, Pharmacology, or a related field.
・At least 7 years relevant experience in pharmaceutical company or in academic research with a good understanding of Drug Discovery and Development.
・Knowledge for drug formulation, ADME, safety or drug delivery is desirable.
・Skills in LBA and/or LCMSMS analysis for engineered small molecules, peptides, ADCs, multifunctional antibodies.
・Experience with laboratory techniques.
・Communication skills (active & passive) in own language and in English.

【歓迎経験】

・Demonstrated expertise in developing and implementing ADME screening methods and establishing SARs for small molecule, antibody, and ADC.
・Experience in drug development and familiarity with cancer therapeutics.
・Experience with animal handling.

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】在宅可、茨城

年収・給与

800万円～　経験により応相談

大手内資製薬メーカーにてグローバルブランドおよび治療領域（TA）コミュニケーションの戦略的リードを求めています。

仕事内容

（雇入れ直後）
Brand/TA Communications
• Serves as the single point of contact for global brand business teams and the Global Commercial Communications network on the brand/TA.
• Helps foster business growth and stakeholder trust/advocacy through a deep understanding and passion for the business, science and data, and by leading co-creation of external brand/TA communication strategies.
• Identifies and applies robust insights to inform effective external brand/TA communication strategies in the co-creation markets.
• Drives effective execution of these strategies through robust planning and relevant content development.
• Enables measurement of meaningful business outcomes for external brand/TA communication strategies in the co-creation markets, strengthening strategies and tactics based on these findings.
• Collaborates with business stakeholders and five markets per brand/TA to co-create effective external brand/TA communication strategies.
• Engages Global Commercial Communications network to ensure broad pull through of external brand/TA communication strategies.
• Supports global, regional and local media engagement through development of Brand/ TA narratives and message maps.
• Leads media training of global brand spokespeople.
• Identifies and executes strategic global media opportunities that will drive strategic Brand, TA, R&D, and company's priorities, including positioning of our Executives as thought leaders.

Issues Management
• Proactively monitors and analyses global media monitoring of brand/TA- related issues that may impact stakeholder trust and Company reputation.
• Provides strategic communications counsel on brand/TA-related issues to the global brand business teams and Global Commercial Communications network.
• Leads communications aspects of Issues Management for global brand/TA-related issues.

Internal Communications
• Leads development and execution of global brand/TA communication strategies that engage and inspire brand teams to deliver for patients, and compay.
• Applies a measurement approach to internal communications.

Overall
• Informs and/or collaborates with Corporate, R&D Communications and IR as appropriate on brand/TA-related communications and issues.

応募条件

【必須事項】

• Bachelor’s or advanced degree in communications, life sciences, business, or a related field.
• Extensive experience in pharmaceutical or healthcare communications.
• Strong understanding of regulatory, compliance, and industry best practices.
• Exceptional written and verbal communication skills, with the ability to simplify complex scientific information.
• Proven ability to manage multiple projects under tight deadlines with attention to detail.
• Experience in a global, matrixed environment is highly desirable.

【歓迎経験】

Global & Multi-Market Communications
• Proven ability to lead and execute global or multi-market brand communication strategies in the pharmaceutical or healthcare industry.
• Strong business acumen and experience aligning communications with commercial objectives in a regulated environment.
• Expertise in coordinating stakeholders across time zones, functions, and cultural backgrounds.

Strategic & Data-Driven Communications
• Ability to translate complex scientific and medical data into clear, engaging, and compliant messaging.
• Experience developing and implementing high-impact communication strategies that drive brand awareness and stakeholder engagement.
• Strong analytical skills to measure effectiveness and optimize communication strategies.

Cross-Cultural & Stakeholder Engagement
• Experience working with diverse, global teams and external partners, fostering collaboration across multiple markets.
• Ability to create inclusive, culturally relevant communications while ensuring compliance with industry and local regulations.
• Proven experience building trust-based relationships with internal and external stakeholders.

Leadership & Execution Excellence
• Experience leading teams and managing complex, multi-market projects in a fast-paced, matrixed environment.
• Strong project management skills, ensuring timely execution and impact-driven communications.
• Ability to manage multiple priorities and drive alignment across global, regional, and local teams.

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】在宅可、東京

年収・給与

800万円～　経験により応相談

大手内資製薬メーカーにて研究企画、戦略策定に関する業務をお願いいたします。

仕事内容

External Ecosystem Engagement:
・Cultivate and maintain strong connections with global academic centers, biotech hubs, incubators, and scientific consortia especially in China.
・Represent Oncology Research at major scientific conferences, innovation forums, and academic meetings to uncover early-stage opportunities.
・Actively track and engage with scientific communities driving innovation in oncology, immuno-oncology, and modality technologies.

Scientific Opportunity Identification & Strategic Insight:
・Monitor emerging trends, novel platforms, and groundbreaking discoveries across oncology and related disciplines.
・Identify high-impact science and technologies with potential to shape the future of research portfolio.
・Translate early-stage innovation signals into pre-transactional strategic insights that support research prioritization, portfolio planning, and exploratory evaluations.

Cross-Functional Collaboration & Knowledge Integration:
・Collaborate closely with Research Strategy Leads, Modality Intelligence Leads, and Innovation Intelligence Analysts to ensure insights are shared and acted upon.
・Partner with Business Development to provide scientific framing and strategic context for external opportunities while maintaining a non-transactional focus.
・Contribute to the development of intelligence infrastructure and best practices for horizon scanning, opportunity mapping, and external engagement across CI & RPM

応募条件

【必須事項】

・Advanced degree (PhD, MD, MBA, or equivalent) in Oncology, Life Sciences, or a related field.
・Minimum 8 years of experience in pharmaceutical R&D, external innovation, academic collaboration, or scientific partnering.
・Strong understanding of oncology drug discovery, translational science, and modality platforms (e.g., next gen ADCs, engineered biologics, engineered small molecules).
・Proven ability to engage with scientific leaders and navigate early-stage biotech and academic ecosystems.
・Excellent communication skills with the ability to synthesize complex scientific information into strategic insights.
・Prior experience in academic liaison, external innovation, or strategic scouting in pharma/biotech or venture ecosystems.
・Familiarity with CI platforms, digital literature monitoring tools, and academic/biotech databases.
・A strong network in academia or biotech focused on oncology or immuno-oncology in China.
・Experience in competitive intelligence, scientific scouting, or innovation strategy within oncology.
・Familiarity with academic-industry collaboration models and consortia-based innovation.
・High digital literacy and comfort with landscape analytics, scientific intelligence platforms, and conference tracking tools.
・Fluency in Mandarin Chinese, along with English, is preferred to facilitate effective engagement with local stakeholders, academic institutions, and innovation partners in the region.

【歓迎経験】

・Demonstrated expertise in developing and implementing ADME screening methods and establishing SARs for small molecule, antibody, and ADC.
・Experience in drug development and familiarity with cancer therapeutics.
・Experience with animal handling.

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】在宅可、茨城

年収・給与

800万円～　経験により応相談

大手内資製薬メーカーにて財務コンプライアンスとガバナンスの担当者を求めています。

仕事内容

（雇入れ直後）
Global & local Business Process JSOX Control Framework Maintenance & Support
• Collaborate with business functions by providing subject matter expertise to identify financial risk and design JSOX controls to mitigate
• Manage and maintain business process JSOX control framework documentation by working with global and regional business functions
• Prepare annual JSOX scope documentation in collaboration with Internal Audit
• Design and lead remediation action plan & resolution of audit inquiries and requests with control performers
• Initiate and drive control performance / ways of working improvements and efficiencies e.g. use of global systems
• Direct Japan JSOX program with necessary decision making while advising global stakeholders of Japan specific JSOX related items
• Principal point of contact for API & ATEC & AKR JSOX compliance related questions

Global & local JSOX Compliance Training program and delivery
• Lead targeted and recurring training program to the control performer community regarding JSOX risk and control performance requirements

Global FC&G Management Reporting
• Report JSOX execution metrics to Senior Management across business functions and regions
• Run meetings with Japan Senior Leadership, Internal Audit, and External Audit regarding compliance results and initiatives

応募条件

【必須事項】

• University degree in Accounting, Finance or related discipline.
• Seasoned Professional with deep knowledge in Financial Compliance Topics
• Business-level English

【歓迎経験】

·Advanced Degree

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】在宅可、東京

年収・給与

800万円～　経験により応相談

大手内資製薬メーカーにて臨床モニター（CRA）を募集しています。

仕事内容

Acts as primary local company contact for assigned sites for specific trials. Trials may include both early and late phase clinical trials.
• Develops meaningful site relationships through consistent collaborative communication and engagement.
• May participate in site feasibility and/or pre-trial site assessment visits.
• Attends/participates in investigator meetings as needed.
• May serve as Regional Sub-/Lead or Global Sub-lead CSM for specific study providing study level oversight and support for CSMs assigned to the study. This assignment ensure study level information is shared with assigned CSMs and has key role in establishing site monitoring strategy for study.
• Responsible for driving activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies. Responsible for the implementation of risk based monitoring approaches at the site level and to work with site to ensure timely resolution of issues found during monitoring visits.
• Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases. Responsible in close collaboration with study team for the activities during site activation phase to speed up the process and activate the site in the shortest possible timeframe.
• Ensure site compliance with study protocol, ICH-GCP, and local/country regulations.
• Ensure ongoing adequacy of site (facilities, staff) for trial conduct.
• Ensure source and other site documentation is adequate and in compliance with ALCOA-CCEA
• Involved with site level recruitment strategy and prioritization and implementation in partnership with other functional areas.
• Ensures site non-IMP study supplies are adequate for trial conduct.
• Ensures that clinical drug supplies are appropriately used, handled, and stored and returns are accurately inventoried and detailed.
• Oversees the appropriate destruction of clinical supplies.
• Ensures site staff complete data entry and resolve queries within expected timelines.
• Ensures validity and completeness of data collected at trial sites.
• Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs) are reported within the required reporting timelines and documented as appropriate.
• Maintains complete, accurate and timely data and essential documents in relevant systems used for trial management.
• Fully documents trial related activities, in particular monitoring. Writes visit reports and follow-up letter in accordance with the SOPs. Promptly communicates relevant status information and issues to appropriate stakeholders.
• Reviews study files for completeness and ensures archiving retention requirements are met, including storage in a secure area at all times.
• Aligns with relevant training requirements. Act as local expert in assigned protocols. Develops therapeutic knowledge sufficient to support role and responsibilities.
• Works closely with CTL to ensure Corrective Action Preventative Action (CAPA) is completed for Quality Assurance (QA) site audits and for quality issues identified at the site during routine monitoring visits.
• Prepares trial sites for close out, conduct final close out visit.
• Establishes and maintains good working relationships with internal and external stakeholders in particular investigators, trial coordinators and other site staff.
• May participate in the Health Authority (HA) and IEC/IRB submission and notification processes as required/appropriate.
• May be responsible for up to 10 sites across 2-4 protocols, dependent on complexity of protocols, site activity and required role in CSM group. Responsible for managing own travel budget within guidelines.
• Oversight the daily activities of junior CSMs. If necessary, communicate with relevant stakeholders and try to find the new approach to avoid any obstacles.

応募条件

【必須事項】

・BA/BS degree with ≥5years of experience in pharmaceutical related drug development or direct equivalent experience.
・Five years site monitoring and/or site management experience.
・A minimum of 2 years of Oncology, Ophthalmology, and/or Gene Therapy or other directly relevant therapeutic area experience.
・Strong working knowledge of GCP, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.
・Strong critical thinking and problem solving skills.
・Strong IT skills in appropriate software and company systems.
・Willingness to travel up to 40% with overnight stay away from home.
・Proficient in speaking and writing English. Depending on hiring region, may also be required to be fluent in local language.
・Good written and oral communication.

【歓迎経験】

・Experience working cross-functionally and in matrix teams
・Experience in executing Lead CSM role
・Experience mentoring more junior site monitors or site managers
・Experience working in early development studies

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】在宅可、東京

年収・給与

600万円～　経験により応相談

大手内資製薬メーカーにてメディカルオペレーターを募集しています。

仕事内容

Oversight and strategic lead for Medical Information function for the assigned therapeutic area. This includes:
•Develop and oversee the strategy or operations of Medical Information function for assigned TA(s) through consolidation of input from appropriate stakeholders with identification of key clinical issues, gaps, and/or process improvements.
•Identify new and innovative solutions to fill the gaps related to Medical Information function, and manage, develop, review, and maintain specific ongoing or new projects or operations regarding Medical Information as assigned.
•Manage, develop, review, and maintain Medical Information projects or operations as assigned. This may include collaborating with product partners and other internal and external stakeholders.
•Contribute to Japan Core Medical Team (J-CMT) as Medical Information representative.
•Contribute to the development and implementation of J-CMP for assigned project(s)
•Bring expertise related to the function to Medical Information group.
•Manage the role allocation and work load in assigned TA(s)
•Document in Global Medical Information Database (GMID) and respond to unsolicited requests from HCPs and patients with appropriate data
•Interpret Medical Information data to generate insights and gap analyses
•Conduct product and process training for contact center vendor staff and other departments as requested
•Monitor Medical Information key performance indicators
•Review standard/custom response documents for medical accuracy and veracity, as assigned
•Collaborate with groups outside MA, Japan (Medical Information global, Patient Centricity, Patient Advocacy, Legal, Commercial, E&C, etc.) as appropriate
•Responsible for active participation on Japan Core Medical Team as assigned
•Verify Medical Information Request Web Forms from the Medical Representatives are unsolicited per applicable country requirements
•Report potential adverse events and potential product complaints per policy and established processes
•Ensures effective communication between internal and external groups regarding Medical Information.
•Works proactively and in collaboration with stakeholders to identify and manage constraints and risks, facilitating resolution
•Ensure compliance and transparency within processes and procedures of Medical Information in alignment with Legal / Regulatory /Compliance
•Develop and maintain compliance relevant to regional legislation, regulations and internal policies.
•Remain current on regional and local regulations.
•Develop and maintain regional quality documents required for local needs, aligning with global quality documents.
•Oversee the outsourced vendor related to the preparation and/or review of promotional/non-promotional material.

Quantitative Dimensions:
•Oversee across multiple products in assigned TA(s)
•Identification of gaps in policy/procedural areas of Medical Information
•Interacts with and influences internal and external stakeholders effectively regarding system and quality document issues
•Direct impacts compliance with: regulatory/safety/legal requirements of the regional regulatory agencies, regional and international pharmaceutical codes, and internal policies
•Fulfillment of escalated unsolicited medical information inquiries, quality monitoring of these activities as assigned
•Handling multiple projects with a high level of efficiency
•Collaboration with global groups, vendors and other colleagues as appropriate for project.

Organizational Context:
•Reports to the Team Lead, Medical Information Escalation-Japan, Global Medical Information.
•Works in a matrix environment; collaboration with leadership and product teams, collaboration with stakeholders at varying levels including, but not limited to Medical Affairs, Commercial, Legal, Compliance, Regulatory and Pharmacovigilance.
•Provides leadership for new and ongoing initiatives across Medical Communications.

応募条件

【必須事項】

•Bachelor’s degree or higher in the field of life science
•At least 3 years clinical practice experience and/or pharmaceutical industry experience
•In depth medical/scientific knowledge of assigned products and TA.
•In depth knowledge of statistics, medical/scientific terminology and medical writing.
•Ability to review/understand complex scientific and medical data from clinical and non-clinical trials and summarize content in both written and verbal forms is needed
•Has excellent understanding of legal/regulatory/compliance requirements and guidelines with respect to Medical Information/ Medical Affairs in the pharmaceutical industry
•Advanced knowledge of the advantages and disadvantages of available medical references and online literature searching
•Excellent oral and written communication skills, presentation skills and basic negotiation skills
•Ability to be logical and strategic thinking
•Basic proficiency in English (written/oral/presentation)

【歓迎経験】

•Experience working on global team or in a global environment
•Advanced proficiency in English (written/oral/presentation)
•Healthcare professional (e.g. pharmacist, nurse) with a Bachelor’s degree or higher.

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京

年収・給与

600万円～　経験により応相談

大手内資製薬メーカーにて抗体研究者を募集しています。

仕事内容

（雇入れ直後）
•Promote/propose engineered antibody/protein programs in the research pipeline in collaborating with internal research groups.
•Discover and design antibodies or protein biologics using biochemistry and molecular biology techniques.
•Develop or conduct multiple in vitro and/or in vivo assays to characterize antibody or biologics profiles using biology expertise.
•Provide ideas to develop innovative antibody drug candidates by utilizing antibody research platforms.
•Lead multiple types of meetings by providing good presentation and facilitation with good communication skills.
•Engage actively with global cross-functional teams and external stakeholders on scientific and strategic direction of research programs to create high value candidates
•Provide best solutions for the objectives in an unprecedented research area
•Ensuring research compliance and integrity

応募条件

【必須事項】

•Ph.D. degree with +3~ years’ experience or MS degree with +5~ years’ experience in drug discovery in pharma or biotech.
•Deep knowledge and expertise on molecular biology or pharmacology.
•Experience of drug discovery research with cross-functional team.
•Good communication and logical thinking skills that can facilitate the relationship with internal colleagues and external (potential) partners in own language.
•Oral and written communication skills in English

【歓迎経験】

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】茨城

年収・給与

800万円～　経験により応相談

GLP組織運営に関する資料保存・管理業務を担っていただきます。

仕事内容

所属：非臨床事業部　創薬レギュラトリーセンター　運営管理室
組織構成：グループリーダー1名、メンバー16名　男性7名、女性9名　平均年齢51歳
募集背景：前任者定年退職予定のため

職務概要：
・試験資料保存に関する契約書の作成、顧客との交渉調整
・資料管理保存業務
・資料返却業務

職務詳細
・GLP施設として各種研究実績等資料の保存を顧客より委託され行っております。保存する資料は多様なものがありシステムを利用した保存管理を行っています。
　実際の紙媒体資料を取り扱い適正な管理を行います。顧客より信頼される業務を行うことが必要です。顧客と資料保存に関する契約、見積手続きを行うことがありご経験のある方は活かして頂きやすいです。
・将来的には資料保存責任者としてGLP施設の信頼に貢献する人材と成長して頂ければ幸いです。非常にやりがいのあるポジションです。

応募条件

【必須事項】

・OAスキル（Word，Excel）
・化学物質過敏症（ホルムアルデヒド等）でない方

【歓迎経験】

・営業等で契約書の作成に慣れている方

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】在宅可、茨城

年収・給与

400万円～600万円　経験により応相談

新製品または特定治療領域に関する製品戦略およびgo to market modelの策定・実行・支援などを行っていただきます。

仕事内容

新製品または特定治療領域に関する製品戦略およびgo to market modelの策定。承認後は営業活動、および販売促進資料の開発を実施する。また、予算編成を支援する。営業チームと緊密に連携して、必要な資料を提供する 等

■マーケティング戦略策定 及び 営業戦略策定の立案・実行
- 市場環境、顧客、製品およびポートフォリオを深く理解し、ブランドチーム、関係部門と協力しながらビジネス課題を特定・構造化・分析し、課題を解決するための製品戦略を立案することに貢献する
- 市場環境の正確な理解、戦略立案のための仮説の検証、打ち手の評価を一次・二次調査により明確にし戦略の検証・改善を行うことに貢献する
- 競合に打ち勝つためのgo to market modelを立案し、実装する

■マーケティング戦略の実行

- 製品戦略に基づく実行プランを自らが中心となり立案・実行・評価まで責任を持って実施する
- 戦略の立案・実行に際して社内外のステークホルダーへ提案し、承認・サポートを獲得する
- 営業部門を始めとする他部門と密に連携をとり、マーケティングプランの伝達を行う
- KEEのマネジメントを円滑に行い、戦略の実行を徹底する

応募条件

【必須事項】

■経験
・3年以上のMRとしての現場経験
・1年以上の医薬品メーカーでのMKT経験

■語学
・日本語 Japanese：Native Level (日本語でのコミュニケーション能力が十分であること)
・英語 English：応募時でTOEIC 600点超
※また、1年以内にTOEIC 730点のレベルまで向上させることを必須とする

【歓迎経験】

・循環器領域での経験
・英語 English：Business Level (to communicate with global team members and external stakeholders)

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】在宅可、大阪、他

年収・給与

700万円～1100万円　経験により応相談

治験および臨床研究等のデータマネジメント（以下、DM）業務を推進いただきます。

仕事内容

・クライアントのDM業務窓口となり、収集データやスケジュールなどの調整、DM要件定義の取りまとめ、　DM計画書作成
・社内の臨床開発部門、プロジェクトマネジメント部門、解析部門との業務連携・調整
・EDCシステムの仕様作成・設計
・DMチェックリスト作成
・データクリーニング、メディカルコーディング（データのチェック・入力はメンバーがメイン）
・プロジェクトにおけるDM業務マネジメントおよび、メンバーマネジメント
・海外子会社のDM業務マネジメント（DM業務の進捗管理、定期会議等）

応募条件

【必須事項】

・大学院もしくは大学卒以上
・理系バックグラウンドであることが望ましい

以下いずれかに当てはまる方
①　製薬企業またはCROにおいてのDM業務経験が5年以上の方　
②　①のご経験とあわせて、以下いずれかのご経験をお持ちの方　　　　　
　　・クライアント窓口業務　　　　　
　　・CROまたはVendorのマネジメント業務　　　　　
　　・クエリ要否判断　　　　　
　　・EDCセットアップ　
③　海外グループ会社 DM部署との連携によるコミュニケーションスキルおよびDMに関する　 　　知見の向上を目指す方

【歓迎経験】

・英語力

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】大阪、他

年収・給与

450万円～650万円　経験により応相談

大手外資製薬メーカーにて、マーケティングやマーケティングサポート業務をご担当いただきます。

仕事内容

1. データ＆分析戦略の立案・推進
・パーソナライゼーション実現に向けたデータ取得・分析計画の策定
・クロスファンクションチームと連携し、必要なデータ・分析手法・ケイパビリティを定義
・分析チームの実行支援と、データに基づく意思決定の促進
・外部委託している機能の評価と、内製化の検討・推進
・オムニチャネル施策の効果測定やダッシュボード設計のリード
・データ基盤の整備や自動化の推進

2. コンテンツのパーソナライズ支援
・コンテンツ・開発チームと連携し、医療従事者の状況やニーズに応じた情報提供を支援
・グローバル戦略・イニシアティブとの連携
・AI、セグメンテーション、タグ付けなどの必要なケイパビリティの整備

3. Next Best Action（NBA）戦略の発展
・NBAツールに関するSME（専門担当者）として、ユースケースの開発・改善をリード
・ローカル・オフショアチームと協業し、課題の明確化とビジネスインパクトの創出
・KPI達成に向けた支援
・類似のNBAツールとの連携・統合に関する戦略的インプットの提供

応募条件

【必須事項】

・オムニ/マルチチャネルマーケティングの実務経験（最低3年以上）: デジタル施策、パーソナライゼーション、KPI設計・評価に関する理解と実践経験
・前例や答えのない課題に対して、自ら仮説や戦略を立てて実行できる能力
・クロスファンクション連携力: 国内外の関連部署との協業を通じて、戦略立案から実行までを推進できるコミュニケーション力
・プロジェクトマネジメント能力: 複数の中規模プロジェクトを同時に管理し、期限内に成果を出す実行力
・クリエイティブ思考と柔軟性: 新しいアイデアの創出、課題解決、革新的なマーケティング戦略の提案力
・コンプライアンス意識: 規制の厳しい業界での業務遂行経験、社内外のルール・法令の遵守力
・日本語・英語での高いコミュニケーション能力

【歓迎経験】

・製薬業界におけるセールス・マーケティング経験
・コンサルティングファームや戦略部門で培った経験を活かした、仮説思考で戦略を設計できる能力
・デジタルメディアの効果測定(Paid / Owned / Earned / Shared)、高い分析能力
・マーケティングプラットフォームの実務知識: Adobe Experience Manager、Google Analytics、Google Search Console、SFMC、などの主要ツールの活用・分析経験

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】兵庫

年収・給与

700万円～1000万円　経験により応相談

大手内資製薬メーカーにてベンダー契約担当者を募集しています。

仕事内容

（雇入れ直後）
• Contract Negotiation: Lead the negotiation of contracts for IT services, ensuring favorable terms and conditions that align with objectives. Partner with IS Business Stakeholders, Vendors, Legal, Procurement, and Compliance teams to reach consensus on contract terms, ensuring alignment with company policies and regulatory requirements.
• Contract Management: Oversee the entire contract lifecycle, from drafting and execution to renewal and termination, using enterprise tools such as ServiceNow, Ariba, and Aravo.
• Requirements Gathering: Work with DigitalX stakeholders to ensure requirements are adequately documented and shared with vendors.
• Vendor Relationship Management: Build and maintain strong relationships with vendors and service providers, addressing any issues or concerns that may arise.
• Team Development: Work with junior members of DigitalX Contracting team to provide guidance on specific contracts, develop their skills, and foster a team environment.
• Risk Assessment: Identify and assess risks associated with contracts and develop strategies to mitigate them.
• Collaboration: Work closely with cross-functional teams, including DigitalX, Procurement, and Legal, to ensure alignment on contract scope, terms, and service delivery.
• Performance Monitoring: Monitor vendor performance against contract terms and service level agreements (SLAs), ensuring compliance and addressing any discrepancies.
• Documentation and Reporting: Maintain accurate records of contracts and related documentation and provide regular reports to management on contract status and performance. Monitor contract timelines for renewals, amendments, and terminations.
• Procure-to-Pay Support: Support Procure-to-Pay processes, including Purchase Order creation/changes and resolution of accounting issues (e.g., funding limits, incorrect coding, etc.).
• Policy Development: Contribute to the development and implementation of policies and procedures related to contract management and vendor relationships.

応募条件

【必須事項】

• Degree in Business Administration, Information Technology, Law, or a related field.
• 5+ years of experience negotiating, executing, and managing IT services and contracts.
• 5+ years of experience managing relationships with vendors, with a strong understanding of vendor governance structure, processes, and best practices.
• Strong negotiation skills
• Strong communication and interpersonal skills, with the ability to build relationships at all levels of the organization.
• Familiarity with relevant legal and regulatory requirements related to IT contracts.
• Proficiency in Microsoft Office tools.
• High-level of Japanese language proficiency, both written and spoken
• High-level of written English language proficiency, intermediate level of spoken English.

【歓迎経験】

• Advanced Degree.
• Consulting Experience.
• Experience working in the Pharmaceutical or other highly regulated industry.
• Experience with ServiceNow, SAP, and data analytics tools.
• Experience working with contract management software and tools, including Ariba.

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京

年収・給与

800万円～　経験により応相談

総合包装メーカーにて品質保証を担当いただきます。

仕事内容

医薬品・治験薬GMPに関すること（社員教育等）やその他栃木工場内の薬事法に基づく品質保証業務をお任せします。
工場での受託包装に関する品質面での確認やお取引先の監査対応などを行い、工場での製造管理・品質管理が適正かどうか、法律や医薬品GMP省令に則した対応ができているかの確認を行います。また社内における品質面のルールを作ることも品質保証の仕事です。
医薬品や化粧品、食品など私たちの生活に身近な様々な製品を取り扱っております。同社にしかできない包装ノウハウを有しており、パッケージを通じて私たちの生活に貢献しています。

応募条件

【必須事項】

・理系学部学科卒業

【歓迎経験】

【免許・資格】

・第一種運転免許普通自動車 必須

【勤務開始日】

応相談

勤務地

【住所】栃木

年収・給与

400万円～500万円　

大手内資製薬メーカーでAIエンジニアを募集しています。

仕事内容

• GenAI Research & Prototyping: Continuously monitor and evaluate new generative AI models and APIs.
• Rapid Proofs-of-Concept: Spin up quick prototypes to benchmark capabilities, latency, cost, and usability.
• Multi-Agent Systems: Design and develop multi-agent architectures to support collaborative AI workflows.
• Fine-Tuning & Domain Adaptation: Prepare domain-specific datasets and fine-tune LLMs (LoRA and full-model) with experiment tracking via MLflow.
• API Integration & Deployment: Design, develop, and maintain secure, scalable integrations with generative AI endpoints (OpenAI, Anthropic, HuggingFace); embed GenAI features into web, mobile, and backend systems.
• Production Support & Training: Provide hands-on support to production teams and deliver training sessions on technical AI concepts.
• Performance Monitoring & Optimization: Define and track key metrics (generation quality, response time, cost per call); implement retrieval-augmented generation (RAG) using scalable vector databases relevance.
• Collaboration & Knowledge Sharing: Partner with product managers, frontend/backend engineers, and data scientists to translate requirements into GenAI solutions; document and follow best practices.
• Stakeholder Communication: Convey complex AI concepts clearly to non-technical audiences.

応募条件

【必須事項】

• Education: Bachelor’s degree in Computer Science or a related field
• Experience: 3+ years of machine learning &or software engineering, with a focus on designing, building, and deploying highly scalable AI solutions
• Programming & Automation: Expert proficiency in Python for API development, automation, and scripting
• GenAI Frameworks & APIs: Hands-on experience with generative-AI APIs (OpenAI, Anthropic, Cohere) and orchestration frameworks (LangChain, LangGraph)
• Fine-Tuning & Experiment Tracking: Skilled in fine-tuning workflows (LoRA and full-model) and experiment tracking tools such as MLflow (or equivalent)
• Model Optimization: Knowledge of model quantization techniques to reduce inference cost and latency
• Retrieval-Augmented Generation: Familiarity with vector databases (and RAG) approaches for improved relevance
• Infrastructure & Deployment: Solid understanding of RESTful and GraphQL services, containerization (Docker), orchestration (Kubernetes), and cloud platforms (GCP, Azure)
• Data Safety & Cost Efficiency: Detail-oriented approach to data privacy, security, and cost optimization
• Collaboration & Communication: Excellent problem-solving skills, clear technical communication, and proven ability to work cross-functionally with product, engineering, and data science teams

【歓迎経験】

• ETL & Data Pipelines: Familiarity with end-to-end ETL processes and tools for data extraction, transformation, and loading
• Scalable ML & GenAI Projects: Proven track record delivering large-scale machine learning or generative-AI applications
• Monitoring & Logging: Solid understanding of application monitoring and logging tools (e.g., Prometheus, Grafana, ELK Stack)
• Databricks: Hands-on experience with Databricks for data engineering and ML workflow orchestration
• MCP (Model Context Protocol): Understanding of MCP for managing model inputs, outputs, and conversational context
• Multi-Agent System Orchestration: Experience designing and managing orchestration of multi-agent AI systems
• Real-Time Connectivity: Expertise integrating real-time data streams and low-latency connectivity in production systems

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】在宅可、東京

年収・給与

800万円～　経験により応相談

内資製薬企業にてEC広告・ECマーケティング担当を募集しています。

仕事内容

・広告運用(ECモール/ECサイト)
・ECモール/ECサイトのデータ分析・施策検討
・DtoC事業の推進
※中心業務は広告運用となります。

応募条件

【必須事項】

・ECモールにおける広告運用経験
・Excel　数式の活用、ピボットテーブル
・Power Point　上長もしくはクライアントへの報告資料作成経験

【歓迎経験】

下記の経験があるとなお可
・ECモールや独自ドメインサイトの管理運用経験
・Amazonにおける広告運用、売上向上施策実施の経験
・LPOによるKPI 改善経験
・Excel マクロの活用(なお可)、スプレッドシートの活用(なお可)
・Power Point　自社、もしくはクライアント企業の意思決定に寄与する提案資料作成経験
・AIによる業務効率化(Gemini なお可)

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京

年収・給与

500万円～700万円　

財務経理部門の次期マネージャー候補として、業務に取り組んでいただきます。

仕事内容

・会計データの入力、管理
・試算表、B/S、P/Lの作成、分析
・予算実績の管理業務
・固定資産の計上及び管理業務
・経理業務全体のプロセス改善
・国税対応及び税務申告書作成

応募条件

【必須事項】

・上場企業での経理経験をお持ちの方
・税務対応のご経験をお持ちの方

【歓迎経験】

・経理部門でのマネジメント経験（2～3名でも可）をお持ちの方

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】大阪

年収・給与

800万円～1200万円　経験により応相談

プロジェクトの範囲と要件について交渉・定義し、プロセス改善やテクノロジーを活用したソリューションを提案

仕事内容

The Senior Principal System Analyst in IT GFS SCM & 3PM Commercial Order Management is responsible for delivering demand management, business consultancy, project management, and IT-related services to designated business stakeholders globally with focus on the APAC region including Japan. This role demonstrates strong capabilities in both project management and domain architecture.

Through continuous engagement with business partners, the analyst identifies and analyzes business needs, negotiates and defines project scope and requirements, and recommends process improvements and/or technology-enabled solutions. The role leads and manages IT projects end-to-end, ensuring alignment with business goals and strategic priorities.

Key responsibilities include：
Partnering with clients to prioritize and govern IT service demands.
Ensuring accountability for the delivery and performance of IT services.
Driving projects to achieve intended business outcomes and measurable benefits.
The successful execution of these responsibilities is expected to contribute significantly to overall business performance.

Additionally, the analyst collaborates closely with IT colleagues and business users to implement IT processes and technology solutions that enhance operational efficiency and productivity.

応募条件

【必須事項】

・5 years+ IT and business experience in the SAP Order-to-Cash (SD module) including documentation and testing
・Accomplished communication and relationship-building skills – you’ve worked with decision-makers, consultant resources and external creative and technical personnel, preferably in a fast-paced and complex project environment
・Proficiency in both Japanese and English

Ability to manage tasks independently
・Experience participating as a team member in projects

【歓迎経験】

・Experience in JIRA & Confluence (Atlassian suite) would be useful, but not essential
・Experience in project management (optional)

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京

年収・給与

600万円～1100万円　経験により応相談

日本拠点のITインフラストラクチャのあらゆる側面の計画、実装、保守、サポートを担当

仕事内容

A statistician (STAT) is a key player of conducting observational/database research in Medical division of . Therefore, STAT surely has the following responsibilities:
・Support/advice and Post marketing DB research from a statistical point of view including research design, Statistical analysis, and sample size calculation
・Assessment of study endpoints/study design/results and interpretation of research results
・Implementation of innovative methodology for prediction or causality

応募条件

【必須事項】

・Master degree in Statistics, Engineering, Science (Math, Physics, informatics) or equivalent
・ (individuals holding MD/Public health/pharmaceutical science degree may be acceptable
・Professional of statistics

経験：
・Statistician/Statistical programming in clinical development
・Research for statistical methodology

スキル：
・Programming skill of R, & SAS in clinical studies
・Implementation of new technology & methodology
・Publication/Medical writing of own researches
・Exchange of insights about statistical subjects with external
・Presentation at meetings about study design, results, and statistical methodology

語学力：
・Read/write statistical documents including study population in English/Japanese
・Communicate, and discuss Statistics/bioinformatics topics with the key stakeholders and experts in English/Japanese practically
・Make a English presentation, organize and facilitate the research/clinical study in the global meetings

【歓迎経験】

In addition to the left mandatory experience,
・Experience in reviewing, assessing and using Real-World data for the research purposes to address clinical / research questions
・Networking, integrating and using EMR(electronic medical records)/EHR(electronic health record) data for the clinical / epidemiological research
・Using / applying bioinformatics methodologies to analyze medical big data / database / scientific research outcomes
・Health Technology Assessment in building models, estimating Health Care resources, analysing the health economics/technology and crafting value propositions
・PhD in Biostatistics

スキル：
・Programming skill of Python
・Lead meeting of which agenda includes statistical topics

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】大阪、他

年収・給与

1100万円～1600万円　経験により応相談

コントラクトMRとして製薬企業の要請を受け、その製薬企業の医薬品に関する適正使用情報の提供を支援

仕事内容

コントラクトMRとして製薬企業の要請を受け、その製薬企業の医薬品に関する適正使用情報の提供を支援

・担当エリア内での訪問医療施設のターゲティング
・担当医療施設への訪問計画作成
・担当医療施設への訪問、医療従事者とのリレーション構築
・卸 MS（Marketing Specialist 医薬品卸販売担当者）とのリレーション構築
・医療従事者向けの説明会の企画・実施
・医師同士のコミュニケーション推進のための研究会・勉強会の立ち上げ
・医師との個別の症例検討・治療提案の実施
・副作用マネージメント
・講演会の企画・運営
・市販後調査

応募条件

【必須事項】

・1.5年以上のMRの経験
・売上および目標達成におけるコミットメント力 （情報を分析し、計画を立て、実行し、確認をする能力）
・コミュニケーションスキル （社内外の関係者との高い関係性を構築・維持することが出来る）
・プレゼンテーションスキル （ターゲットに対して効果的な説明を行うことが出来る）
・PCスキル初級（顧客管理データの作成、レポートの作成、プレゼンテーション資料の修正等）
・全国勤務可能な方（初任地はご相談ください）
・4 年制大学卒業（文系・理系など学部は問いません）


※46歳以上及び勤務地限定の方は、契約社員となります。

【歓迎経験】

【免許・資格】

MR認定資格・普通自動車運転免許有

【勤務開始日】

（7月1日）応相談

勤務地

【住所】東京

年収・給与

600万円～1050万円　

AI・デジタル変革推進リーダーとして、組織の戦略的変革を主導するポジションです。

仕事内容

・AIおよびデジタル変革ロードマップ策定・実行、AI ソリューション開発・導入（プロコード／ロー・ノーコード）、ビジネス分析による業務改善やROI評価
・社内外との連携：グローバル・ローカルの関係部署との連携、外部パートナー/ベンダーとの協働
・チェンジリーダーシップ：メンター・トレーニング、デジタル文化醸成、プロジェクトリーダーとしての推進
・責任範囲：戦略企画提案、PPM（プロジェクト＆ポートフォリオ管理）における改革、成果報告、リーダー層への提言
・Formulation and execution of AI and digital transformation roadmaps. Development and implementation of AI solutions (pro-code/low- and no-code). Business analysis for process improvement and ROI evaluation.
・Collaboration with internal and external stakeholders: Partnerships with global and local departments, and cooperation with external partners and vendors.
・Change leadership: Mentoring and training, fostering a digital culture, and promoting initiatives as a project leader.
・Scope of responsibilities: Proposing strategic plans, driving reforms in project and portfolio management (PPM), reporting results, and making recommendations to senior leadership.

応募条件

【必須事項】

経験
・企業または組織のデジタル変革・AI導入プロジェクトでのリード／推進経験（目安5年以上）
・ビジネス分析や業務改善・アウトカム測定の経験
・戦略企画・立案およびプロジェクト実行で成果を出した経験
・複数部門やステークホルダーとの協働経験
・AIソリューション実装経験（プロコード：Python、R、Java等／ロー・ノーコード：Copilot Studio、Power Platform等）
・Experience leading or driving digital transformation and AI adoption projects within companies or organizations (around 5+ years).
・Proven experience in business analysis, process improvement, and outcome measurement.
・Demonstrated success in strategic planning, proposal development, and project execution.
・Collaborative experience working with multiple departments and stakeholders.
・Experience implementing AI solutions (pro-code: Python, R, Java, etc.; low/no-code: Copilot Studio, Power Platform, etc.)

資格
・情報科学・工学・データサイエンス・経営学・情報システム等の学士号以上
・Bachelor’s degree or higher in Computer Science, Engineering, Data Science, Business Administration, Information Systems, or related discipline.

能力
・業務課題抽出力とビジネス分析力
・戦略的思考と変革推進力
・高度なコミュニケーション能力（経営層、部門横断的な提案・調整）
・AIガバナンス・コンプライアンスに関する実務知識
・Ability to identify business challenges and perform business analysis
・Strategic thinking and transformational leadership
・Advanced communication skills (across executive management and cross-functional proposals/coordination)
・Practical knowledge of AI governance and compliance

語学
・日本語：レベル不問
・英語：ビジネスレベル（社内外ステークホルダー、グローバルコミュニケーションに対応）
・Japanese：Any
・English：Fluent (able to communicate with internal external stakeholders globally)

【歓迎経験】

経験
・製薬・ライフサイエンス・先端技術領域におけるR&D関連の実務経験
・グローバルプロジェクト／多国籍チームとの連携経験
・外部ベンダーやAI技術パートナーとの協働経験
・Hands-on R&D experience in the pharmaceutical, life sciences, or advanced technology sectors.
・Experience collaborating on global projects and working with multinational teams.
・Proven track record of cooperation with external vendors and AI technology partners.

資格
・AI・データサイエンス・プロジェクトマネジメント関連資格（例：PM資格、AI関連認定等）
・Qualifications related to AI, data science, and project management (e.g., project management certifications, AI-related certifications, etc.)

能力
・外部ベンダーやテクニカルパートナーとの調整・管理能力
・メンター、トレーナーとしてのチーム育成・文化醸成経験
・多様性・インクルージョン推進の取り組み経験
・Ability to coordinate and manage external vendors and technical partners
・Experience in mentoring, training, and fostering team culture
・Experience promoting diversity and inclusion initiatives

語学
・日本語：ビジネスレベル（日本R&Dチームとの円滑なやり取り）
・Japanese : Fluent (Smooth communication with the Japan R&D team)
・Location：Osaka or Tokyo

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】大阪

年収・給与

1200万円～2000万円　経験により応相談