Jobs list of Pharmaceutical
-
Job number: Job-00222648 Posted: 2023-07-03
Business Planning Manager,
Sales planning80 - 120 million yen Tokyo Pharmaceutical Sales / MR
- Company overview
- This company is one of the world’s leading pharmaceutical companies.
- Responsibilities
- Market analysis and strategy development:
Japan strategy development, annual plan and 5 years plan
Market assessment by applications, in close collaboration withrelevant stakeholders
New market/application trends analysis
Commercial Execution initiatives:
Performance management (KPIs monitoring)
Sales channel management(including e-commerce, digital, data analytics)
Drive project implementation and executions of selected initiatives across PS Japan organizations
Commercial Operations:
Direct responsibility for meeting/activities objectives and agendas
Support sales data and information analysis
Collaborate with controller for financial analysis/KPIs for
-
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
-
Job number: Job-00259434 Posted: 2024-01-18
海外薬事開発アソシエイトディレクター
研究開発薬事経験が活かせます。15 - 15 million yen Tokyo Pharmaceutical Marketing
- Company overview
- Our client is conducting research and development in regenerative medicine.
- Responsibilities
- 心筋細胞および膵島細胞の両開発資産に関するグローバル規制戦略の策定を主導
BUヘッドをサポートし、グローバルに申請データパッケージをデザインする
FDAなど海外の規制当局と協議する際に、CMCデータパッケージやIND申請のための前臨床データパッケージの適切性、規制当局の主張をサポートするための試験デザインなど、あらゆるトピックについて責任ある橋渡しとなる。
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加速の可能性を含む規制関連事項のプレゼン、ディスカッションを社長と直接連携して行う
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する
-
Job number: Job-00255489 Posted: 2023-10-19
薬事マネージャー
医療用医薬品のGVP/GQP、RAに関する幅広い知識をお持ちの方必見です14 - 17 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- -
- Responsibilities
- 1. マーケティングコンプライアンスオフィサー(総括責任者) 安全管理責任者および品質保証責任者の監督・指導を通じて、GVPおよびGQPの遵守を保証する責任を負う。
問題やリスクをMAHに報告する。
2. レギュラトリー・アフェアーズ(RA) 日本におけるRAの当局対応窓口。
コーポレートRA部門から送付される文書の科学的な内容だけでなく、法規制に準拠しているかをチェックする。
変更、更新、新規製造販売承認申請を所轄官庁に提出する。現地の要求事項に従って関連書類を添付する。
申請中の承認のフォローアップを担当する。当局から要求があった場合、質問に回答し、追加書類を提出する。書類の承認状況をコーポレートRA部門に報告する。
現地規制情報を担当する。日本の新規制についてコーポレートRA部門に情報を提供する。
日本の薬事法に関する専門知識・知見に基づき、薬事戦略を提案する。
医薬品の包装材やSmPCの改訂・検証を行う。
-
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
-
NEWJob number: Job-00266089 Posted: 2024-03-28
Pricing & External Affairs Senior Manager
Pricing Senior Manager position at global mega pharma12 - 18 million yen Tokyo Pharmaceutical Market Access / Pricing / HEOR
- Company overview
- This company is the world\'s leading pharmaceutical company.
- Responsibilities
- ResponsibilitiesDevelop strategic NHI pricing strategies and gain endorsement of NHI pricing strategies and proposals of NHI prices with Country President and TA Leads through the Pricing Committee
Develop robust pricing dossiers and strategically manage price negotiations
Build strong alignment & partnership among Japan Pricing Core members (New Asset & Access Strategy team, New Asset Analysis team, DJ, Medical, Launch Excellence Team, Policy and Public Affairs, and the global PHI) to ensure optimal price setting
Develop Pricing-related OP assumptions
Refresh pricing assumptions and estimated prices for pipeline products and BD assets to reflect the latest competitive environment
Minimize the downward price adjustment by price revision/repricing through cross-functional collaboration
Maintain good relationship with “Policy Planning Division for Pharmaceutical Industry Promotion and Medical Information Management, MHLW” (former EAD) and act as a mediator between the company and MHLW to flawlessly manage all product-related issues, as well as NHI pricing negotiation
Actively participate in trade association activities (FPMAJ, PhRMA, FIRM, etc.) to establish a pro-innovative pricing framework
Contribute to building a high performing team by actively engaging in coaching junior colleagues and nurturing a positive environment where people feel energized and eager to speak up
-
NEWJob number: Job-00266093 Posted: 2024-03-28
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
-
NEWJob number: Job-00208873 Posted: 2024-03-25
Digital Marketing Project Manager
Digital PM12 - 16 million yen Tokyo Pharmaceutical Marketing
- Company overview
- This company is one of the world’s leading pharmaceutical companies.
- 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.
-
Job number: Job-00211156 Posted: 2023-06-15
Senior Manager Clinical Research
Global position12 - 18 million yen Tokyo Pharmaceutical Clinical Development
- 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
- Create Japan clinical development plan within global development strategy
Lead clinical studies in Japan from scientific perspective
Lead PMDA consultation related to Japan clinical development
Develop clinical study protocols
Support development of other study-related materials (e.g. draft Informed Consent, Case Report Form, study related SOP, etc.)
Support study operations
Perform medical monitoring of clinical study data
Develop Clinical Study Reports
Lead clinical related part of approval review
Develop clinical sections of the Common Technical Document (CTD)
Develop responses for clinical related inquiries
Make presentations at scientific meetings and/or author manuscripts on clinical trials, or provide necessary support for them
-
Job number: Job-00203644 Posted: 2023-10-04
Medical Doctor - Safety
1st MD position in the company12 - 18 million yen Tokyo Pharmaceutical Pharmacovigilance
- Company overview
- Our client is a global IT service company that provides a wide range of solutions to help businesses transform their operations, enhance customer engagement, and drive growth in today\'s digital economy
- Responsibilities
- Perform second level triage workflow, review through the entire source document for any potential serious adverse event/s in the case based on conventions
If the case is serious, then in the activities tab, select the Case level seriousness as Yes
After the review of the case, document the assessment in the same action item, To be retained as Non-serious OR To be upgraded as Serious with respective rationale and close the action item
Inform the respective triage associate via email for upgraded case
Ensuring the ICSR is medically relevant, complete and accurate
Validation of Seriousness criteria, events captured, coding, labeling, Causality assessment, Writing Company / PV comment. Review and finalize Narratives.
Generating medically relevant follow-up questions
Identifying and notifying potential signals
-
Job number: Job-00204324 Posted: 2024-03-08
【東京】Head of Genito-Urinary Marketing
オンコロジー・マーケティング経験者必見です!12 - 18 million yen Tokyo Pharmaceutical Marketing
- Company overview
- Our client is one of the most well-established European-based international pharmaceutical companies in Japan.
- Responsibilities
- 長期、中期、短期の事業戦略とマーケティングプランを策定し、GUエリアにおける同社製品の販売ポテンシャルを最大化する。
市場調査能力を確立し、実行することで、市場領域を定義し、ターゲットとなる医師や医療機関を選定して市場領域の定義、ターゲットとなる医師・医療機関の選定、市場ポテンシャルの推定、競合他社の分析、医療・治療ニーズの現状と将来をビジネスに反映させるための現在および将来の医療および治療上の要求をGU製品のビジネスに反映させる。
短期的な全国レベルのマーケティングプランを実現し、効果的な広報活動と広報・情報施策(会議、ミーティング、販促資料など)を用いた短期的な全国レベルのマーケティングプランを実現する。メディカルアフェアーズ/マーケットアクセスと協力して、タイムリーかつ利用可能な方法で提供する。
研究開発およびグローバルオンコロジーチームと協力して、収益と利益の最大化を実現するために、GU製品のライフサイクルマネジメントを計画、実施する。R&Dおよびグローバルオンコロジーチームと協力して、収益と利益の最大化を実現するために、GU製品のライフサイクルマネジメントを計画・実施する。
-
Job number: Job-00203537 Posted: 2023-11-29
MD
2nd in MD to be hired in JP12 - 15 million yen Tokyo Pharmaceutical Medical Doctor
- Company overview
- Our client is a clinical-stage biotechnology company.
- 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.
-
Job number: Job-00203429 Posted: 2023-06-15
Clinical Trial Leader
Managing all clinical activities12 - 17 million yen Tokyo Pharmaceutical Clinical Development
- Company overview
- This company is one of the world’s leading pharmaceutical companies.
- Responsibilities
- Leads the development of the clinical trial strategy and delivers the clinical operational plan within the budget, timelines and quality standards agreed upon by Governance Committees.
Accountable for oversight of CROs in the execution of Phase I – III global clinical trial(s).
Represents Global Clinical Operations (GCO) within the Global Trial Team and serves as the key GCO operational point of contact for the trial.
Accountable for the successful preparation and presentation of operational content at key governance discussions
Key contributor to the development of annual trial/project objectives and communicating to relevant line management and Clinical Operations Team
Drives and leads the successful execution, oversight and approval of all clinical trial documents and operational plans of global clinical trials using strong project management, leadership, and organizational skills.
Ensures strong oversight, review and delivery of trial/project CAPAs in order to meet corporate compliance standards and timelines.
Accountable for partnering with CRO in audit responses and addressing quality issues.
Provides leadership and contributes to all operational aspects of the trial budget, including forecasts to ensure delivery within the R&D financial standards.
Performs review and provides strong operational input in the development of clinical trial protocols, ICFs and CSRs and contributes as a member to the CTM Internal Protocol Review Committee.
Filters, prioritizes, analyzes and validates complex and dynamic information from a diverse range of external and internal sources to respond to technical operational and organizational challenges.
Supports the development and implementation of department initiatives including input on SOPs, processes, and workstreams.
Ensures strong inspection readiness application for all assigned clinical trials.
Manages a small project or project stream with tasks of low to moderate complexity within a larger project. Leads a small project team with members typically from direct working environment and a straightforward project structure. Coordinates stakeholders from own area or even closely related areas or is partially or even fully responsible for the project’s management within small to medium sized projects. Applies technical expertise in the analysis of factual information and may even look beyond the immediate problem and use business acumen to understand the wider implications.
Accountable for projects within a clearly defined scope and milestones. Receives moderate to low level guidance and direction within broad guidelines.
-
Job number: Job-00203430 Posted: 2023-10-11
Senior Manager, Regulatory Manager
Managing two different teams12 - 17 million yen Tokyo Pharmaceutical Regulatory Affairs
- Company overview
- This company is one of the world’s leading pharmaceutical companies.
- Responsibilities
- Effective manage regulatory pathway for Life Science (LS) products and services in Japan, cover the areas of biopharma processing, pharm & food materials (APIs, pharmaceutical excipients, food additives), medical devices, IVDs, equipment/instrument, biologics and animal derived materials, etc.
Drive thought leadership initiatives and build up relationship and advocacy with local authorities and industry associations in terms of Life Science interests. Safeguard company strategic interests and objectives in arising guidance, standards and regulation.
Monitor and report on changes of relevant regulatory and compliance environment with impact with the Life Science business. Analyze available regulatory and compliance information.
Effective coordination of strategic activities with the company subject matter experts, local regulatory bodies and industry associations. Secure flow of information from/to authorities, industry associations and the Life Science organization.
Training and support to internal stakeholders, external customers and relevant regulatory bodies. Provide relevant training to educate local marketing/sales colleagues about new regulatory trends and developments that drive our value proposition. Definition of processes to implement upcoming regulatory needs and requirements.
Closely work with global/regional regulatory surveillance & advocacy team and regulatory subject matter experts to link the local advocacy activities with global/regional advocacy activities.
Drive, manage and coordinate registration / notification / listing activities in Japan. Ensure the correctness and timeliness of these activities, interim follow-up change management and final outcome. Ensure tracking, maintenance and reporting of registration / notification / listing status.
Provide regulatory guidance in risk assessment, identify regulatory impact to the Life Science and provide regulatory recommendations to mitigate potential risk. Take active role to represent company in delicate or risk potential matters with regulatory agencies, inspectors and trade associations.
Provide regulatory support to marketing, sales and customers via consultation, seminars and training events.
-
Job number: Job-00203431 Posted: 2023-07-03
Senior Clinical PMS Manager
In charge of all clinical PMS12 - 17 million yen Tokyo Pharmaceutical Clinical Development
- Company overview
- This company is one of the world’s leading pharmaceutical companies.
- Responsibilities
- Accountable for day to day activities of all aspects of the operational management of local post-marketing studies (PMCT and PMS), including study timelines, resources, allocation and management of product (re-) supply, problem identification and resolution, status reports and budget to ensure timely delivery of completed study reports to the project teams
Accountable for the oversight of investigator-initiated studies granted by the company, including the support of the set-up and operational assessment of investigator-sponsor, tracking performance and payments according approved plan, managing product supply, if applicable, coordinating internal review of final report
Manage independent consultants including CROs, clinicians, independent CRAs, or statisticians when required by the project including selection, coordination of project specific training, and payment
Develop and monitor study budget and timelines
Monitor work to ensure quality
Ensures that trial status is tracked and entered into the respective Clinical Trial Management System
Contribute to the planning and set-up of a study and provide planning parameters
Overseeing external providers, Act as an interface between Global Clinical Operations and local organizations (Global Operations)
-
Job number: Job-00261920 Posted: 2024-01-18
安全対策・メディカルドクター
癌領域の専門性や経験をお持ちの方必見です。12 - 16 million yen Tokyo Pharmaceutical Medical Doctor
- Company overview
- Our client is Global Leading Pharmaceutical Company.
- Responsibilities
- 抗がん剤の開発プロジェクトへの参画もしくは上市後間もない抗がん剤を担当し、以下の安全対策業務に従事する。
副作用・有害事象症例の安全性評価と臨床試験における安全対策の検討
RMP(医薬品リスク管理計画)等の安全対策の立案・実施
安全対策に関する当局との交渉(承認申請時の対応含む)
重大な副作用発生時におけるKOL(Key Opinion Leader)や使用医師等との専門性に基づく円滑なコミュニケーション
治験時のベネフィットとリスクバランスの評価および安全確保措置の立案・推進
医療機関からの問い合わせに対する対応
-
Job number: Job-00259606 Posted: 2023-12-01
グループマネージャー
製薬・バイオテクノロジー企業におけるバイオ医薬品で少なくとも1年以上のCMC経験をお持ちの方必見です。11 - 14 million yen Kanagawa Pharmaceutical Research & Development
- Company overview
- Our client is conducting research and development in regenerative medicine.
- Responsibilities
- iPS細胞由来細胞製品の製造プロセス開発(製法改良、スケールアップ、工業化)戦略の策定
iPS細胞由来細胞製品の製剤設計及び臨床試験サイトへの輸送戦略の策定
CMOへの製造移管業務のリード及びGMP製造の管理業務
規制当局とのCMCに係る面談等の準備及びそのリード
治験申請資料作成等のCMC関連文書作成業務
製造グループメンバーの業務及び勤務管理
-
Job number: Job-00259608 Posted: 2023-12-01
アソシエイトディレクター
バイオ/製薬業界での研究開発/医療プロジェクトマネジメント経験5年以上の方必見です。11 - 14 million yen Tokyo Pharmaceutical Marketing
- Company overview
- Our client is conducting research and development in regenerative medicine.
- Responsibilities
- 組織のあらゆる中核機能を徹底的に理解し、同社ビジョンに沿った戦略的・戦術的イニシアチブを効果的に管理する
CMOおよびCMOと協働するCSOを支援し、経営委員会またはBCOが承認した計画に従って、すべてのパイプラインの業務執行を監督する
事業部門が主導するプロジェクト開発計画のパイプライン事業遂行を支援。CMOに沿った医療チームの構築・強化のための戦略的計画を策定。その後のコミュニケーションと実施計画の策定。目標、目的、スケジュールの設定を通じて、この計画が確実にモニターされるようにする。
BU横断的な共通プロセスの維持など、その他のパイプライン業務サポート。(薬事関連、非臨床関連を含む)
事業目標の成功に影響を及ぼす可能性のある問題の積極的な特定。CMOが認識すべき問題を提起し、問題解決/問題解決のためのアイデア、リスク軽減のためのアイデアを構築/提示する。
-
Job number: Job-00209039 Posted: 2023-06-15
[Tsukuba] Manager of Venture Unit Tumor-directed inhibition
Global Company!11 - 14 million yen Other Pharmaceutical Research & Development
- Company overview
- Our client is a global pharmaceutical company with its own distribution channels around the world.
- Responsibilities
- Design and synthesize target molecules and analyze assay data for effective drug design as a medicinal chemist
Participate in program-related meetings and contribute to the progress of the program through useful suggestions and discussions
Be coordinated with researchers in a chemistry team as well as with multiple expertise such as biology, ADME and toxicology
Ensure daily experiments to be complied with internal and external laws, regulations, and compliance standards
-Manage partnership/CRO to promote a research program effectively
-
Job number: Job-00263709 Posted: 2024-03-21
Senior Marketing Manager
Marketing Manager position at global phamaceutical maker11 - 14 million yen Tokyo Pharmaceutical Marketing
- Company overview
- Our client is an international pharmaceutical company.
- Responsibilities
- Global pharmaceutical manufacturer is seeking an experienced Senior Manager Marketing. As the company plan s to reorganize the marketing department and expand the team, this role will play a critical role in driving commercial marketing initiatives and shaping brand strategies.
Responsibilities:Lead the development and implementation of commercial marketing strategies to drive brand growth and market penetration.
Collaborate with cross-functional teams to develop comprehensive product launch plans, including product positioning, market research, and branding strategies.
Conduct market analysis and competitive intelligence to identify market trends, opportunities, and potential risks.
Drive the development of branding plans and marketing campaigns to enhance brand awareness and ensure consistent brand messaging globally.
Collaborate closely with Marketing Director and other senior managers to align marketing strategies with overall business objectives.
Provide strategic guidance and support to product teams throughout the product lifecycle, from development to commercialization.
Ensure compliance with regulatory requirements and company policies in all marketing activities.
Monitor and analyze marketing performance metrics to track the effectiveness of marketing campaigns and initiatives.