Total 15 Health / Beauty / Fitness job vacancies in Yotsuya, Tokyo

The Medical Science Liaison (MSL) is a therapeutic specialist who serves as a key field-based scientific resource and technical expert contributing to establishing Clinigen as a leading medicines access company.  This role supports launched medicine and developing medicine throughout Japan, for a range of therapeutic areas (Podiatric, rare diseases).  The position operates within a team structure and will require regular interaction with commercial, marketing, regulatory team and other departments.  This position requires a willingness to contribute to both strategy and tactics with a proactive and can-do attitude.

Key Accountabilities:

• KOL / Investigator / Academia / Scientific community relationships
• Customer Insights
• Knowledge and Compliance
• Medical Information
• Administration

Major Tasks & Activities:

KOL / Investigator / Academia / Scientific community relationships

• Identify, develop and maintain peer-to-peer collaborations and relationships with key medical experts in relevant therapeutic areas.
• Collaborate with physicians and drive medical affairs initiatives including publications, investigator sponsored research (ISR), advisory boards, medical education opportunities, training development programs.
• Provide medical and scientific input into the planning and execution of advisory boards and work with physician experts to review speaker presentations and provide medical references where requested.
• Conduct landscape mapping activities to develop a deep understanding of current patient care in target therapeutics areas.
• Study Group management on the launched product’s post-marketing-surveillance.

Customer Insights

• Collect and communicate key customers insights to internal teams.
• Serve as scientific peer-to-peer resource to disease experts in applicable therapeutic areas. Support the medical community with up-to-date medical information, robust disease expertise and product information when an unsolicited request is received.
• Serve as internal expert in specific therapeutic area demonstrating up-to-date and high-level therapeutic expertise. Train Clinigen staff on key scientific and medical topics in relevant therapeutic area.
• Solicit and share best practices to enhance team productivity.
• Attend and support at International and local congresses / symposia (if needed or required by the needs of the business).
• Deliver, quality medical education presentations in a variety of settings and obtain feedback that can be disseminated throughout the organization e.g. staff meetings, round tables, hospital meeting activities in collaboration with the commercial staff.
• Create and update disease awareness sites to improve patient understanding.

Medical Information

• Deliver medical information responses to all internal and external customer enquiries (escalated from call centre).
• Contribute to and ensure maintenance of the Medical Information Database FAQ, Standard Responses, resources.
• Maintain an up-to-date knowledge of Clinigen products and available resources.

Knowledge and Compliance

• Maintain compliance with all internal and external legal and regulatory guidelines.
• Maintain a current and comprehensive knowledge of Clinigen and competitor's products.
• Maintain up-to-date knowledge of industry trends, cutting-edge practices and techniques, current publications and regulations.
• Maintain up-to-date knowledge of Clinigen’s standard operating procedures and policies and ensure compliance at all times.
• Ensure your Company related activities comply with relevant Acts, legal demands and ethical standards.

Administration

• Ensure documentation is up-to-date and compliant with standard processes and formats.
• Complete required reports within designated timeframes.
• Participate in meetings as required.
• Liaise with management and staff to ensure projects are conducted efficiently.
• Communicate with staff & management using proper channels.
• Master computer skills and required software programs.

• Medical / PhD / Pharmacology / Science Degree
• Previous Medical Affairs, or MSL experience desirable
• Advanced understanding of a relevant therapeutic area(s) e.g. Oncology, Rare Diseases (preferred)
• Understanding of the Medicines JPMA Code of Practice
• Experienced in establishing relationships with senior healthcare professionals
• Demonstrated analytical skills and a solid understanding of research methodology
• Demonstrated ability to effectively communicate across all customer levels, in range of contexts
• Good oral, writing and reading skills in English
• Will be required to travel nationally

• Competitive base salary
• Annual performance bonus
• Ongoing professional development
• Flexible working arrangements
• Supportive team environment

We have a fabulous role for skilled Recruitment Program Specialists to make their mark, supporting a very exciting program within the medical space!  Are you on the move and looking to be a part of the AGS growth story?

It's an opportunity you don't want to miss!

The key focus for the job holder is to lead the successful fulfilment of open vacancies with relevant hiring managers and to be the first point of contact for their hiring needs within the contingent workforce management space (inclusive of contractors/dispatched/Haken employees), whilst being the conduit between the client and your supplier partners.

This is a key role that requires a strategic, engaging, influential, and organized recruitment professional to deliver best-in-class client servicing, program and operational services.

Your Opportunity

• Assist hiring managers during all stages of the contingent hiring process including requisition intake, sourcing, and candidate shortlisting and interviewing.
• Demonstrate recruitment expertise by preparing insightful questions appropriate for the position before conducting a req intake session with the hiring manager, to gather detailed job descriptions to distribute to your supplier partners (recruitment agencies). Additionally, document req intake conversations in the appropriate vendor management system (VMS: Fieldglass or Beeline).
• Utilise reports to manage open requirements to advise managers on the status of requirements and monitor supplier sourcing strategies to ensure timely response.
• Discuss with the Hiring Manager to set/manage expectations, timeframes, feedback, roles, and responsibilities of everyone involved in the requisition fulfillment process.
• Coach, manage, and oversee the performance of participating supplier partners.
• Document all client/supplier reported issues and track resolution through to completion ensuring a high level of customer satisfaction in the appropriate system/tool.
• Monitor performance against contract SLA’s, requisition aging, invoicing, time and expense entry, and vendor compliance tracking.
• Maintain and update monthly activity and performance reports.
• Provide constant interaction via face-to-face, email, and phone with stakeholders (hiring managers, client, suppliers and other partners).

JOB OVERVIEW

The Senior Directory for Lifestyle (Fashion and Living/ Food Beauty & Care) is responsible for developing and executing a long-term business strategy for each of the sub-categories (Apparel, Accessories, Footwear, Home Décor &Bedding, Food Beauty & Care) that leverages the richness of NBCUniversal’s entertainment content (past & present) to build a sustainable business that achieves annual revenue targets.

As part of the Universal Brand Development team, the Senior Director of Lifestyle (Fashion and Living, Food Beauty & Care) will be responsible for growing the CP business in line with divisional strategies and guidelines while leveraging a strong knowledge of the local markets’ individual needs and opportunities. He/she will be responsible for identifying the best licensees to partner with (and approving all business deals), driving innovative and quality product ranges, providing regional input into Global deals, accurate quarterly forecasting and direct management of DTR relationships.

KEY RESPONSIBILITIES

Strategy:

• Set and execute a long-term business development strategy for each Lifestyle category that takes into account regional opportunities and specificities.

Financial:

• Manage the Lifestyle P&L to deliver (or exceed) annual revenue targets. Provide quarterly business forecasts to evaluate progress against budget. Highlight any upsides or sensitivities.

Category Management:

• Develop a clear growth strategy for each category of business (including financial targets) and benchmark progress.
• Identify opportunities and fill gaps by product sub-category, age segment, market channel and franchise.
• Ensure clear & timely communication of Lifestyle strategies and assets with agents.
• Partner with the Creative & Brand Assurance team to drive quality and champion innovation in local product development. Ensure timely product approvals in line with industry needs.

Licensee Management:

• Responsible for developing and managing a portfolio of licensing agents and licensees to grow the Lifestyle business. Critically evaluate the agent and licensee base to ensure we have the right amount and best quality partners.
• Direct management of key Global & Regional licensees.
• Negotiate the best deals (in line with CP guidelines and business objectives) and manage the process from contract to product development and execution. Provide input into global deals to ensure regional needs are met and leverage global deals locally.
• Determine where DTR relationships could enhance our business and negotiate/manage these deals.

Franchise Development:

• Develop a clear franchise growth plan for your region for all of the core properties and identify market-specific opportunities
• Brief additional creative assets where required to meet market needs

Retail Development:

• Work with the Franchise marketing and retail team to identify the key retail partners for your region. Develop relationships with the decision makers at your Key Accounts.

• Understand key seasonality and important dates on the retail calendar

We have an exciting role for our next Recruitment Program Specialist to make their mark, supporting a very exciting program within the medical technology space!

It's an opportunity you don't want to miss out!

The key focus for the job holder is to lead the successful fulfilment of open vacancies with relevant hiring managers and to be the first point of contact for their hiring needs, whilst being the conduit between the client and your supplier partners.

This is a key role that requires a strategic, engaging, influential, and organised recruitment professional to deliver best-in-class contingent workforce services.

AGS社は下記業界の会社をサポートできる採用に関する人材を募集しています。

• ライフサイエンス
• 医療機器
• テック ご

自身のスキルを活かして、弊社を共に成長させていきませんか？  競争力のある給料、いい企業文化、キャリアアップの機会などのベネフィットはもちろん期待できます。

当ポジションに興味がある方、是非ご応募をお待ちしています。

Responsibilities

• Assist hiring managers during all stages of the contingent hiring process including requisition intake, sourcing, and candidate shortlisting and interviewing.
• Demonstrate recruitment expertise by preparing insightful questions appropriate for the position before conducting a req intake session with the hiring manager, to gather detailed job descriptions to distribute to your supplier partners (recruitment agencies). Additionally, document req intake conversations in the appropriate vendor management system (VMS: Fieldglass or Beeline).
• Utilise reports to manage open requirements to advise managers on the status of requirements and monitor supplier sourcing strategies to ensure timely response.
• Discuss with the Hiring Manager to set/manage expectations, timeframes, feedback, roles, and responsibilities of everyone involved in the requisition fulfillment process.
• Coach, manage, and oversee the performance of participating supplier partners.
• Document all client/supplier reported issues and track resolution through to completion ensuring a high level of customer satisfaction in the appropriate system/tool.
• Monitor performance against contract SLA’s, requisition aging, invoicing, time and expense entry, and vendor compliance tracking.
• Maintain and update monthly activity and performance reports.
• Provide constant interaction via face-to-face, email, and phone with stakeholders (hiring managers, client, suppliers and other partners).

JOB DESCRIPTION:

JOB SUMMARY

Reporting to Customer Service Manager, this individual will support daily activities relating to order receiving – order entry, invoicing , customer feedback, and working closely with other functions to address and resolves issues.

Also, monitor outsource team performance and support training if required.

In addition, as part of  order entry automation , will play important role of EDI expansion and analysis.

Major Responsibilities

General:

Customer Service

• Own order process, collaborate with outsourcing team, and carry out stable order processing.

• Coordinate with other departments and manage product control, shipping restrictions, backorder support, etc. related to order processing.

• Accepting inquiries regarding orders from customers (Dealers)

• Examining the efficiency of the order process for Capital products

• Work closing with sales and marketing teams, regulatory, global planning, and local supply chain team striving to provide and accurate demand signal

• Proposal and implementation of order processing efficiency improvements in collaboration with other departments

• Support for smooth operation of product phase-out and phase-in

• Drive action on the short UBD, inactive Inventory, phase-in/phase-out, communicating with business partners to minimize the negative cost impact

• Resolve customer’s complaints to customer satisfaction and proactively seek to identify root cause to prevent reoccurrence.

SAP Master and System control

• Maintain Master of supply chain related SAP

• Organizing SAP system requirements(ITDR), making requests, and conducting tests.

• Determine and maintain EDI parameters in  EDI order convert system.

Compliance with audit rules

• Complying with Abbott Policies

• Follow compliance and Medical Device requirements (Regulatory Affair)

• Providing materials and explaining work content during Sox audits and other audits(Including Abbott policy）

Reporting

• Utilize reporting tools (BO, BW, Power BI, Data Mart and SAP)

Continuous Improvement

• Initiate continuous improvement for driving improvement of work quality, efficiency and accuracy in customer service

• Provide trainings to team members to enhance quality of work

Minimum Requirements

Education:

• Bachelor’s degree or equivalent

Background:

• 1-5 years of working experience in similar roles

Language:

• Business level English /Japanese communication skills required. (e.g. TOEIC 700+)

Preferred Requirement

• Proficient or experienced user in the following IT environments: SAP CRM, ECC and GTS, Business Objects, Business Warehouse ,MS Excel & Access.

• Additional system knowledge welcome/ e.g. VBA macros, power BI

The base pay for this position is

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

DIVISION:

LOCATION:

ADDITIONAL LOCATIONS:

WORK SHIFT:

TRAVEL:

MEDICAL SURVEILLANCE:

SIGNIFICANT WORK ACTIVITIES:

The MSL role is field based customer facing role, activities should be Key medical expert (KME) focused with the intent to maximize medical one on one interactions with HCPs.  Over70% field-related activities (face to face and virtual) is expected in the role.

What You’ll Do

• Acts as a scientific expert knowledgeable of Biogen products, disease state and competitors
• Establishes long term scientific/strategic relationships with leading specialists (physicians nurses, allied health), and with related medical societies and academic centers of excellence
• Ensures KMEs and organizations have access to relevant scientific information
• Facilitates KME involvement in educational forums and advisory boards to optimize scientific knowledge exchange
• Serves as an important partner to internal stakeholders through communication of relevant information

PrimeVigilance is looking for a number of Medical Information Associates to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries in English combined with one of the following languages: Mandarin or Cantonese

Responsibilities 

• To provide approved responses to medical enquiries (healthcare professionals, patients, pharmaceutical clients) including call handling  
• To accurately identify, document and report adverse events/side effects, pregnancy and other special situation events, and product quality complaints within required timeframes 
• To ensure that all medical information enquiries are tracked and fully documented within the Medical Information database accurately and completely 
• To participate in the out-of-hours provision of medical information for clients who have contracted a 24/7 enquiry handling service 
•  Providing management with regular updates regarding project status and metrics concerning enquiries 
• Assisting in departmental regulatory inspection preparedness for the company pharmacovigilance system and actively participating in PV inspections or audits;  

Contribution as a non-clinical medical writer in his/her expertise mainly non-clinical parts for all regulatory documents (CTD, briefing document for consultation, etc.) and positive involvement in strategic regulatory discussion during entire drug development process and also J-NDA from submission to approval for Biogen's programs.

Key Responsibilities:

• Preparation of CTD in module 2 (non-clinical parts) and module 4 as well as some parts of module 1
• Preparation of briefing document (BD) for PMDA Consultation regardless informal and formal
• Preparation of response documents to PMDA questions during approval review, PMDA consultation, etc.
• Preparation of non-clinical inspection by regulatory authorities in Japan
• Communication with global teams to get necessary information and supports
• Vendor management necessary for all document preparation including translation and edition

Job Description

クリニカルリサーチ領域（オンコロジー以外の領域：ジェネラルメディスン・感染症・ワクチン）での以下の業務を担当：

＜医学専門家として＞

・ 開発チームの一員として、開発案件に対する医学専門家としてのアドバイス、文書（治験実施計画書や申請資料等）の医学的レビューを行う

＜日本の開発プロジェクト責任者として＞

・米国本社と連携して、本邦での臨床開発計画の立案・作成、 臨床試験の実施、製造承認の取得

・日本のサイエンティフィックリーダーとのscientific exchange、関係構築

・本邦で実施する治験の医学的／科学的側面からリード

・治験に関する学会発表及び／又は論文作成、あるいはそれらのサポート

職務経験

・医師免許をお持ちの方

・5年以上の医療現場での臨床経験（必須）

・チーム間の協力を促進する能力

・英語での交渉力、スピーキング、ライティング力

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Shift:

Valid Driving License:

Hazardous Material(s):

■仕事内容

• 医療用医薬品の販促に関わる広告・パンフレット・ポスターなどの企画から制作に伴うコピーライティング全般をお任せします。
  ※企画、コピーライティング、制作、編集まで一貫して携わります。
• 医師/薬剤師/看護師などの医療従事者に向けた、臨床効果/作用機序など、製品の特性を捉えたパンフレットの作成を行います。
• 制作業務は、医薬品の申請書や海外文献を読み込んだり、シンポジウムへの参加やドクターへの取材などを行ったりします。
• 新薬の場合、競合プレゼンで取扱いが決定後、発売約1年前から企画、広告ビジュアル･パンフレット等の販促マテリアルの制作を開始します。
• 担当する製品だけでなく、競合薬剤や疾患、治療に関する専門知識を身に付けることが出来、ご自身のスキルアップが可能です。

As a member of our Solution Consulting team, you will have a major impact on our future success by supporting Sales team. You will guide revenue for our IT operation management products with the support and partnership of Sales, Product Management, and the executive team. This is a hands-on technical consultant who can go wide and deep on solution delivery and solution positioning during sales cycles.

What you get to do in this role:

The Solution Consultant is a technical consultant with the advanced ability to develop, position and provide product-specific solutions during sales cycles while achieving quarterly and annual sales goals for an assigned territory.

• Advise customers/prospects to take advantage of the ServiceNow IT Operations Management suite to solve business issues and technical problems preventing them from achieving their goals.
• Inspire with an innovative mindset by guiding the future of our ITOM solutions.
• Bringing our customers to higher operational level through proposing AI Ops to prevent impact and automate resolutions.
• Take a leading role in creating and sharing best practices and content both to educate colleagues and help customers realize value faster.
• Qualify, scope, plan and deliver customer-facing activities such as presentations, demos, and proof of concepts.
• Promote and educate about ServiceNow technology and industry trends through public, customer, and marketing events such as conferences, webinars, executive briefings, etc.
• Be the voice of the customer and provide feedback to help product management and engineering teams shape the roadmap and better support our customers.
• Be the go-to person in an area of focus for market trends and competitive analysis with special skills in differentiation for our ITOM solutions.
• Be the trusted advisor for our ITOM solutions for customers, the market, partners, and colleagues, and with a consultative mindset, coach them towards the value-based decisions.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

【部門紹介】

Medical Writing部門では、国内外の製薬会社・ベンチャー企業等から、幅広い治療分野の業務を受託しているため、様々な文書作成に携わり、非常に多くの経験をすることができます。また、社内の教育システムも充実しており、新規案件に対して専門的なアプローチが可能な体制になっています。

【アピールポイント】

・医薬品、医療機器、再生医療等幅広い分野の開発品目に関する文書作成を経験できます
・文書作成に際し、社内の医師や薬事の専門知識を有する者からアドバイスを受けることできます
・グローバルメディカルライティングのメンバーとしてグローバルな環境で仕事をすることができます

【業務内容】

メディカルライター（担当者）として次のような業務をお任せします。

・臨床試験関連文書（治験実施計画書、治験総括報告書、コモンテクニカルドキュメント等）の作成
・グローバル試験の治験実施計画書に対して日本要件を満たすための修正版の作成
・製造販売後調査関連文書（安全性定期報告、再審査申請資料等）の作成
・臨床研究報告書・論文の作成
・各種文書のQC　他

【必須要件】

・Medical Writing実務経験がある（翻訳のみの方は対象外）
・理系大学、大学院卒
・薬学･医学的な基礎知識を有する
・医薬品開発全般、GCP、ICH関連ガイドライン、国内薬事規制(GPSP等)を理解している
・英語の読み書きが可能（辞書を使って英文書の添削や和文英訳が可能なレベル）
・Fluency in Japanese would be required

【歓迎】

・臨床薬理の知識、経験がある方
 

【勤務地】

品川／大阪

【選考ステップ】

　面接2回、筆記試験（文書QC・英文読解、辞書等の使用可）

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

• Support execution and implementation of Regulatory strategies, including adhering to project timelines and prioritizing deliverables.
• Responsible for generating and delivering documentation for life cycle management and registration of products domestically.
• Coordinates the assessment of product changes to capture any impact on existing or in-process product registrations and letters to file.
• Coordinates and documents regulatory activities for clinical studies as needed.
• Assist in submission activities for new product approvals and maintenance of on-market products, and may include support for pre-submissions, Premarket approvals (PMAs), Conformity assessments, IDE submission, Annual Reports, Export certificates, etc.
• Ability to negotiate with PMDA/MHLW to bring submission/approval effectively.
• Ability to work in a fast-paced environment and maintain a “focused urgency” as specific events require.
• Ability to work cross-functionally and communicate regulatory requirements to project teams as needed.
• Assists in implementing department procedures and regulatory processes.
• Acquire and maintain current knowledge of applicable regulatory requirements and scientific/technical issues relevant to assigned projects in the geography and discipline.
• Effectively communicate updates on assigned projects and changes in the regulatory landscape to team members and managers.

Quality Assurance and Safety Management

• Collaborate with related functions and be responsible for maintaining and configuring QMS and ISO13485 in accordance with change control processes.
• Lead the company's compliance activities according to PMD Act/ISO13485/15189 and applicable requirements.
• Maintain both QMS and GVP under MAH, including Shonan laboratory.
• Conduct internal audits and top management reviews based on the regulations.
• Communication with the regulatory authorities and notified bodies regarding safety information.
• Collect and manage safety information and lead necessary action.
• Report and respond to related regulatory authorities.
• Ensure that all SOPs are written following applicable regulatory and company requirements.

Regulatory Affairs

1. Responsible for activities that lead and maintain regulatory promotion code for In Vitro Diagnostic (IVD) devices, medical devices, and RUO products.
2. Support to create and review a submission package and product insert.
3. Lead QMS assessment regarding submission of new products to PMDA
4. Maintain and manage FMR with collaborating GHI.
5. Lead the company's compliance activities according to the PMD Act/Promotion guideline/ Fair Competition Code and applicable requirements.
6. Maintain and change control MAH and IVD sales license.