バイエル薬品株式会社/医療経済&アウトカムス研究 プロジェクトリーダー / Project Leader//HEORの求人【バイオ転職ナビ】

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医療経済&アウトカムス研究 プロジェクトリーダー / Project Leader//HEOR 人気求人 急募求人  /  バイエル薬品株式会社

ジョブNo.NJB1035272
職種 医療経済&アウトカムス研究 プロジェクトリーダー / Project Leader//HEOR
社名 バイエル薬品株式会社
業務内容 1. Lead the planning, development, implementation, and communication of relevant health economics,health outcomes (e.g., patient-reported outcomes), or real world evidence strategies to support relativevalue demonstration and product differentiation for Bayer products.
2. Work proactively and collaboratively with related internal functions to develop value proposition and toidentify data/evidence requirements for HTA body /each product priority, and execute HEOR researchstudies to meet requirements in order to support brand strategies, market access, pricing andreimbursement.
3. Manage the implementation of HEOR studies, value messaging and scientific communication plans,outputs through congress presentations and publications, and support the development of customer facingdissemination tools.
4. Develop relationships and work closely with key opinion leaders and academic researchers throughoutthe research/dissemination cycle.
5. Work with clinical teams to plan that appropriate health economics/outcomes information is collected inthe course of clinical trials.
6. Serve as internal resources for continuous education regarding concepts commonly defined throughhealth economics and health outcomes research principles (e.g., cost-effectiveness analysis, budget impactanalysis, patient-reported outcomes, and patient preference)
7. Represent Japan on Global HEOR
8. Attend industry meetings as assigned to keep abreast of key market developments
【出張】Depends on projects but as an avarage 2~4 times / months
求める経験 【学歴・経験】
Academic degree (graduate degree preferred) in economics, biostatistics, outcomes research, epidemiology,public health, health services research, pharmacy, medicine or other related fields

【職務に必要な能力・スキル・資格等】
Fluency in both Japanese (JLPT N1 ~ native level) and English (TOEIC 900 or more)
Strong research methods, complex data analysis skills and ability to develop and implement related strategicrecommendationsStrong verbal and writing communication skills (830 Toeic)
Excellent conceptual, analytical, and problem-solving skills
Ability to work collaboratively in team environment, as well as ability to work independently with minimal directionResearch skills
語学力 英語力:中級
勤務地
東京都
年収 650万円 - 1300万円
雇用形態 正社員(期間の定めなし)

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Product Manager_Bone

<Main purpose of Job> Marketing Manager position leading bone osteoporosis access marketing initiatives and programs for romosozumab. Candidates must have a proven track record of sales success and/or marketing experience developing and implementing a wide range of high-impact marketing tools and programs. <Responsibilities> Contributes Japanese Brand Plan development Manages the relationships with co-promotion partners to maximize the value of co-promotion scheme Develops and executes sales promotional activities in alignment with co-promotion partners Coordinates and leads meetings with co-promotion partners Engages and involves sales leadership in planning and key initiatives Develops programs and tools for optimal sales force effectiveness Partners with the Medical Communication Manager in the development and execution of the Medical Affairs and Promotional Program Establishes regular contacts with key opinion leaders Develops regional congress plans Collaborates with colleagues in other Expansion Markets and corporate office as needed on joint projects.

Study Manager, Clinical Operations (炎症・免疫)

<Summary/Scope> The Study Manager provides strategic and operational leadership of clinical research studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, JGCP, Regulatory Authorities’regulations/guidelines, and applicable SOPs/WPs. Responsibilities may include operational direction of one or more cross-functional Japan study team(s) and/or performance and quality oversight of one or more Contract Research Organization (CRO). Study manager has full responsibilities for studies led by the Japan Study Team. Responsibilities in the global study is complied with Affiliate Involvement Model (AIM), Job aid and direction given by Global Clinical Trial Manager (CTM). Responsibilities involve a combination of execution and oversight-dependent on the sourcing model - to ensure deliverables and may include, but are not limited to, the following: -Financial Planning and Management ・Strong understanding of the cost drivers, attuned to principles of cost disciplined science and are able to proactively manage the study budget ・Takes ownership and accountability for the development/management/reconciliation of overall study budget(s) ・Development/management of vendor scope of work (SOW) per contract, quality, and budget ・Review/approval of vendor invoices and management of accruals and SOW changes ・Review/approval of site invoices and management of site budget -Project Management ・Drive study execution ・Oversight of clinical monitoring quality and adherence to established processes and plans ・Development, management, maintenance of study deliverables [i.e. timelines, study plans, etc.] through collaboration with internal and external stakeholders using data and strong inter-personal influencing skills to make robust data driven decisions ・Proactive identification of potential risks and development/implementation of actions to avoid or mitigate and able to make the appropriate trade-offs of balancing risks with study deliverables and costs. ・Maintenance/updating of data as appropriate in project management tools including CTMS ・Informing operational program lead/s and other leadership (as appropriate) on overall clinical trial plans, updated forecasting, and of potential issues/mitigation -Study Planning and Conduct ・Facilitation of site feasibility/selection processes with use of robust data ・Operational and strategic input into study documents such ……(以下詳細は面談時にご案内します)

薬事(管理職)

<担当する仕事内容の詳細> ・承認申請書類、届出書類等の薬事監査 ・GVP、GQP自己点検 ・製造販売中止製品の承認整理、後発医薬品の薬価基準収載手続き及び削除 ・薬事規制の対象となる添付文書、製品のパッケージ、広告等の監査 ・薬事規制に係る情報等の収集・分析及び関係部署への情報提供 ・薬事に係る相談と助言等

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