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3 listing(s) available.

  • 20 Feb 2019

    Scientific Advisor (Neurology)

    Japan

    Permanent Position
    Abbvie - アッヴィの歴史は医薬品業界の先駆者的存在である米国アボット社から始まりました。 アボット社は1888年、シカゴの医師Dr. Wallace Abbottによって設立されました。 以来、アボット社は、150ヵ国以上で革新的な医薬品、栄養製品、診断用製品および医療用製品を人々に提供しながら、医療界のグローバルリーダーとして進化しています。

    Job Description

    Summary of Job Description: 

    Reporting to the Therapeutic Area Associate Medical/Scientific Director, this position represents the affiliate’s medical/scientific voice of expertise for assigned product(s) 

    and relevant therapeutic areas. The position provides medical / scientific expert advice / guidance to key internal and external customers for assigned products and relevant therapeutic areas, 

    including scientific exchange and professional relationship development with external experts. 

    It provides medical / scientific input into marketing strategy and key commercial initiatives, as required, 

    and medical / scientific support for medical department activities under the direction of the Therapeutic Area Medical/Scientific Director.



    Major Responsibilities: 

    ・Develop and maintain in depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / 

    participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature. 

    ・Provide expert medical/scientific advice for assigned products and related therapeutic areas, 

    including responding to requests for scientific/technical information; contribute to the development and 

    medical and scientific accuracy of core dossiers generated by the medical department. 

    ・Establish and maintain professional and credible relationships with external experts and academic centers; 

    this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion forums, etc. 

    ・Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups 

    (meetings, clinical sessions, etc.), where requested. Develop and update medical education materials. 

    ・Screen relevant literature and other information from relevant scientific societies meetings and conferences and 

    develop summaries of key messages for use within the Company (e.g. key areas of scientific/company interest, 

    new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.) 

    ・Contribute scientifically to training to sales forces and other departments; develop and update relevant training materials. 

    ・Clinical Research Activities: 

    -Design and implement clinical research projects within defined standards and budgets 

    (e.g. Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies). 

    -Provide the required oversight to manage review, approval and conduct of IIS studies. 

    -Support the affiliate Clinical Research Department in the management of clinical studies, 

    as appropriate (e.g. review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys). 

    ・Review and preparation of promotional material. Ensure the medical/scientific content is correct and fully compliant 

    with AbbVie’s internal policies and guidelines. 

    ・Provide medical/scientific input into marketing strategy and key commercial initiatives, 

    as required. Monitor the environment for competitive intelligence (e.g. product strategies, studies, commercial messages, positioning, etc.) 

    and communicate, where appropriate, within the Company. 

    ・Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, 

    policies and procedures and accepted standards of best practice. 

    Expires on 28 Apr 2019

    Posted By

    Miki Nagai (少しでも、ご興味お持ちの方はお気軽にご連絡ください。 事前に職務経歴書(英語版、日本語版でも可)を 表記のメールアドレスまでご送付いただけますとスムーズです。)

    Tel: 080-1118-4497

    nagai.m@peoplesearch.jobs

    Requirements

    【必須(MUST)】


    Essential Skills & Abilities: 

    - Knowledge of medical science and regulations – Required 

    - English communication skill – Required 

    - Experience of clinical practice and basic research – Desirable 

    - Experience of job in pharmaceutical company – Desirable


    給与:前職考慮のうえ決定します

  • 20 Feb 2019

    オンコロジーメディカルアフェアーズ メディカルアドバイザー

    Japan

    Permanent Position
    MSD - グローバルヘルスケアリーダーMerck & Co., Inc., Kenilworth, N.J., U.S.A.の一員として、日本の皆さまに医療用医薬品やワクチンをお届けし、革新的なヘルスケア・ソリューションを提供しています。強固なパイプラインと世界140カ国以上で事業を展開するグローバルなネットワークを活かし、未だ満たされていない日本の医療ニーズに積極的に応えていきます。

    Job Description

    Role Overview:
    Oncology Medical Affairs
    The Medical Advisors(MA) is responsible for the medical strategy of the product, provides medical and scientific expertise to maximize medical communications.
    The MA is the responsible person to lead the indication team and develop/execute Country Medical Affairs Plan (CMAP).
    The MA is the Scientific expert and Key person to manage the complete products life cycle management by proactively involving all required stakeholders (Science Hub)

    Key Accountabilities:
    Medical Strategy
    Identify Medical Needs and Data Gaps and lead the preparation and implementation of the medical strategy (including launch strategy) in alignment with all stakeholders (Marketing, Global Medical Affairs, Development, Oncology Scientific Affairs) documented in the country medical affairs plans (CMAP). 
    Communicate with the global functions in regards of the product lifecycle management and global alignment of the medical strategy
    Insights evaluation and management through Scientific Leader (SL) interaction 
    Develop and Manage the CMAP and SL engagement List in collaboration with Medical manager, MSL and MI.
    Build and maintain relationships with important SLs (Local and Global) through scientific interactions (Scientific discussion) and peer-to-peer communication.

    Data Generation
    Plan data generation (DG) strategy to maximize the scientific value of products in line with the local medical and brand strategy.
    Lead local DGs from scientific and strategic viewpoint , as well as execute non-intervention post-marketing studies as the responsible person in collaboration with working-level colleagues as needed.

    Internal Expert & Collaboration
    Educate and inspire medical affairs staff to have the highest scientific standards
    Give proactive scientific and medical direction to MI and MSL: lead the Medical Affairs product related scientific activities
    Support Sales force training upon request from Oncology Business Unit.
    Act as a bridge between clinical development and commercial teams: lead the cross-functional medical activities.
    Review external documents on their clinical/scientific adequacy to deliver a balanced message based on scientific evidence

    Expires on 28 Apr 2019

    Posted By

    Miki Nagai (少しでも、ご興味お持ちの方はお気軽にご連絡ください。 事前に職務経歴書(英語版、日本語版でも可)を 表記のメールアドレスまでご送付いただけますとスムーズです。)

    Tel: 080-1118-4497

    nagai.m@peoplesearch.jobs

    Requirements

    必須条件:
    Medical Affairs部門にてMedical Strategy立案・実行の経験を有する方
    英語ビジネスレベル

    望ましい条件、資質: 
    Medical Affairs部門にてMedical Strategy立案・実行の経験を有する方(Oncologyの経験があることが望ましい)

  • 15 Feb 2019

    Medical Advisor / 泌尿器癌 or 血液癌

    Japan

    Permanent Position
    IQVIA - ヘルスケアの発展に寄与する医療情報、テクノロジー、分析力および人知による創意工夫を活用した幅広いソリューションを提供しています。日本法人として当社は唯一無二の医療データベースと最先端のテクノロジーをもとに、エビデンスに基づくインサイトを結集して、医療ステークホルダーの課題解決に寄与し、医療の発展と最適化に貢献します。

    Job Description

    Medical Monitoring: 
    l Primarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on assigned projects. 
    l Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility. 
    l May contribute to the medical review of the protocol, Investigative Drug Brochure (IDB) and/or Case Report Forms (CRFs). 
    l May provide therapeutic area/indication training for the project clinical team. 
    l Attends and may present at Investigator Meetings. 
    l Performs review and clarification of trial-related Adverse Events (AEs). 
    l May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. 
    l May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department. 
    l May perform medical review of adverse event coding. 
    l Performs review of the Clinical Study Report (CSR) and patient narratives. 
    l Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested. 
    l Available 24 hours per day, 7 days per week to respond to urgent protocol-related issues at the investigative sites.

    Expires on 28 Apr 2019

    Posted By

    Miki Nagai (少しでも、ご興味お持ちの方はお気軽にご連絡ください。 事前に職務経歴書(英語版、日本語版でも可)を 表記のメールアドレスまでご送付いただけますとスムーズです。)

    Tel: 080-1118-4497

    nagai.m@peoplesearch.jobs

    Requirements

    【必須(MUST)】

    ・MD licence
    ・Clinical Experience in Oncology-Urology in Japan
    ・Current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in applicable therapeutic area. 
    ・Good communication, presentation and interpersonal skills, including good command of English language (both written and spoken). 
    ・Ability to establish and maintain effective working relationships with coworkers, managers and clients. 
    ・Attention to details, ability to provide advice on multiple assignments and flexibility. 

    給与は前職考慮の上で決定いたします

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