腎細胞がんまたは、頭頸部癌メディカルリード /メディカルアフェアーズ 【製薬オンライン】製薬会社・製薬メーカー・製薬企業・医薬品・医療機器等の製薬・医療業界の求人転職サイト

受付時間 平日9時~20時まで 土曜9時~17時まで 03-6278-8721

製薬業界専門の転職・求人サイト 製薬Online.com
最終更新日: 2018年 04月 20日
春の転職支援キャンペーン 期間:2018年1月26日(金)から4月30日(月)

求人情報

メディカルアフェアーズ

求人管理No.012294

会社概要

腎細胞がんまたは、頭頸部癌メディカルリード

Direct interaction with external stakeholders and medical science liaisons to refine and adjust unmet medical needs to external environment

募集要項

Proactively and continuously identify Unmet Medical Needs (UMN) related to assigned products based on the regular dialogue with Thought Leaders(TL), advisory board meetings, published information (domestic/overseas books/journals/congresses)and other available information (statistics, epidemiology etc)

Data Generation:
・ Identify data gap for the assigned product between the available data and ideal data set to satisfy the UMN, to promote appropriate use of the assigned product, and to maximize the patients’ benefit.
・ Strategically and creatively develop a data generation plan from scratch to fill the data gap taking feasibility, scientific adequacy, and ethical considerations into account. This can include post-marketing trials (PMT), request for proposal (RFP) of investigator-sponsored researches (ISRs), and corporate-sponsored researches (CSRs).
・ Explain, discuss and align the data generation plan with internal stakeholders (Brand team, Executive Management, Global Medical etc).
・ Implement the data generation plan including ISR request handling (interface to investigators, representative of toward global team).

Publication:
・ Strategically develop a publication plan of the assigned product including original papers and congress presentations focusing on company-sponsored clinical trials (Ph.1~Ph.3, Ph.4 if applicable)and get endorsement from J-EDT/J-FDT/Global Medical.
・ Implement publications with targeted schedule. This includes story building, communication with external/internal authors and reviewers as well as medical writer, contents validation, and on-time delivery of the publication.
・ Update the publication plan according to the clinical trial progress, UMN and competitive landscape and get endorsement.

TL engagement:
・ Support identifying TLs according to objective and transparent definition. Maintain and update the TL list at least annually.
・ Track interactions and maintain relationship with TLs in a completely compliant manner with related procedural documents (PD).
・ Peer-to-per discussion about products based on the individual needs of the TL/HCP: - Scientific information: -Treatment option: -Clinical research
・Collecting, storing, processing and distributing medical insights for strategic areas: - Local treatment practice: - Ongoing clinical trials (competitor) - Competitor products perception: - UMN
・ Answer unsolicited request (on & off label)
・ Deliver medical presentation to TL (one-one & group presentation)
・Identify TL / Speaker / investigator / Advisor
・ Help speaker in slide/lecture preparation
・ Approved interactions with MKT, Commercial, RMS and MR
・ Help investigator to understand ISR submission
Medical Education
・ Identify the needs for medical education based on UMN to promote appropriate understanding and use of the assigned product.
・Plan on medical educational meetings/printed materials/other communications considering adequacy and feasibility, and implement them.
Medical Plan Management
・ Creatively develop Medical Plan annually from scratch integrating UMN, data generation, publication, TL engagement, medical education, and any additional activities along with a given global template and policy accompanied by a concrete budget plan. Update the Medical Plan at budget update cycle.
・ Effectively and efficiently explain the Medical Plan and get endorsement from Executive Management in as well as Global Medical.
・ Completely understand internal PDs, other rules, and laws and regulations in Japan. Assure that Medical plans and its implementation comply with these rules/regulations/laws.
Cross-functional business lead
・Lead medical matrix team (consists of functions in JMAP)and align each activity with the Brand Team activity. Co-lead the brand team with Senior Product Manager. Participate in J-EDT/J-FDT from medical and scientific viewpoint.
・ Lead negotiation on the meeting for the alliance of co-development and co-promotion with strengths the high scientific information
・Through medical events, such as non-promotional scientific events, advisory board meeting or scientific consortium, exert the leadership in cross functional team-meetings based on new proposal.

募集条件

  • ・Knowledge of assigned therapeutic area (disease mechanism, epidemiology and typical treatment in Japan) at specialized physician’s level.
    ・Knowledge of the assigned products covering CTD Module 2.4 ~ 2.7 and 5.3.5 as well as all publications including the latest one.
    ・Basic knowledge about clinical development (Ph1-4), ISRs, Japanese PMS and matrix organization .
    ・Knowledge about Medical Affairs Law, Fair Competition Code (FCC), Promotion Code, and any other applicable regulations in Japan.
    ・Skills to analyze information (TL interactions, surveys, public information), identify needs/risks, translate them into an integrated medical plan, and implement it with regular monitoring and issue management.
    ・Communication skills as a professional in Japanese context, both internally and externally.
    ・Team management skills to lead a team, nurture trust and confidence among members, and identify and address issues in a team.
    ・One year or more experiences in Medical Affairs in Japanese industry preferred.
    ・Three years or more experiences of research in medical, pharmaceutical or life-science field preferred.
    ・Two years or more experiences in assigned therapeutic area preferred
    ・MD, Veterinarian Doctor or PhD in medical/pharmaceutical/veterinarian/life-science area preferred
    ・First author for at least an original paper (PubMed-cited level) and a congress presentation preferred
    ・Complete level of written Japanese- can completely understand medical articles and general business documents in Japanese, can write formal Japanese at business setting, and can write a medical article in the assigned area.
    ・Complete level of oral Japanese - can have medical discussions and build an appropriate relationship with HCPs
    ・Advanced level of written English - can completely understand medical articles of assigned area and general business d

勤務開始日

  • 応相談

雇用形態

  • 正社員

勤務地

  • 東京

転勤有無

  • 当面なし

勤務時間

  • フレックスタイム制度あり

給与

  • ご経験に応じての額となります。