• 常勤
  • 東京都

【東京都港区】外資系大手製薬メーカーMA

MSL, Eyecare

  • 300423903
  • 2026年10月05日更新
  • 当直なし
  • オンコールなし
勤務地 東京都港区
給与(年収) 1200万円 応相談
募集科目 眼科、その他、製薬会社
交通アクセス ***
医療機関区分 その他会社
病床数 ・・・
屋内の受動喫煙対策 敷地内禁煙

この求人に問合せる無料

この求人に問合せる無料

求人情報

勤務内容・条件

募集科目 眼科、その他、製薬会社
勤務内容 その他
対象専門科目:眼科

仕事内容:
Objectives:

Medical Science Liaisons (MSL) will ensure that proper relationships with both established and emerging external experts (EEs) in Ophthalmology and Eyecare disease treatment are developed and nurtured ,and that our scientific credibility is advanced as planned. This position is based in Tokyo and will report to the MSL Manager, Eyecare.

Key Responsibilities:

Develop and maintain key scientific knowledge for credible dissemination of Eyecare and Ophthalmology related scientific information to external experts and healthcare professionals.
Identify qualified external experts to engage with in collaborative efforts such as Advisory Board meetings, medical educational programs, congress symposia and potential research collaborations.
Conduct with high integrity infield activities as determined by the annual medical functional plan and properly document outcome of scientific engagements with targeted external experts.
Provide scientific support to and maintain relationships with targeted external experts in Eyecare area including key academic societies by delivering credible scientific presentations through individual or in group interactions.
Provide external ophthalmic surgical experts with scientific and technical support to ensure ophthalmology surgical devices are properly used in clinical settings.
Work with local Medical Information as appropriate to ensure responses to the unsolicited scientific requests including off-label information on medicines are accurate, up to date, reviewed and approved by local relevant internal and external procedures.
Act as the point of contact for potential investigators by facilitating the communication with Area/Global Medical team on investigator-initiated study (IIS) ideas related to products and/or pipeline assets.
Attend scientific meetings/conferences and develop summaries of key data presented to be shared with the Brand Team and other internal stakeholders.
Comply with all applicable local and international laws and regulations, guidelines, codes of conduct, standards, policies and procedures.
Work cross-functionally with commercial and other internal stakeholders as needed to achieve the Brand Team business objectives.
Attend all assigned training courses to acquire and update job related knowledge and skills.
Upon request, assist prescribers with requests for access to medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory requirements.
週勤務日数 5.0日
勤務時間 (月~金) 08時45分 ~ 17時30分
週5日(月~金曜日)
8:45-17:30 (休憩時間60分)
フレックスタイム制(コアタイム無 フレキシブルタイム5:00~22:00)
当直 なし

待遇・手当

給与(年俸) 1200万円 応相談
赴任手当 -
住宅手当 -
宿舎の提供 -
自動車通勤 -

福利厚生

休日 日曜日、祝日、土曜日
休暇 年末年始、その他休暇、初年度有給休暇
研究日 なし
社会保険 健康保険、雇用保険、労災保険、厚生年金
学会出席 -

その他

試用期間 あり(3カ月)同条件
備考 勤務地:東京都港区
年  収:1200万円~(目安)※経験・スキルによります。
契約期間: 無期雇用 
雇用形態: 正社員 
試用期間: 有  期間〔3ヶ月〕 
就業時間: 8:45~17:30 (実働7時間45分)フレックスタイム制:有(コアタイムなし /フレキシブルタイム5:00 – 22:00)
時間外労働: 有 
休日休暇: 原則として土曜日、日曜日、国民の祝日、年末年始、その他会社が指定した日 [年間休日合計126日]
年次有給休暇:毎年1月1日付で付与・入社初年度については、入社月により按分
その他休暇: 特別有給休暇、生理無給休暇、産前産後休暇、子の看護休暇、介護休暇、など 
福利厚生: 健康診断・人間ドック、各種オプション検査、奨学金プログラム(子女)、災害・経済的困難時支援プログラム
慶弔金・見舞金制度(結婚祝金、出産祝金、弔慰金、傷病見舞金、災害見舞金)、団体扱契約生命保険、団体契約損害保険
死亡・高度障害補償(総合福祉団体定期保険、損害保険)、労災上乗せ補償(法定外補償保険)、GLTD(Group Long Term Disability:長期休業補償)制度企業年金制度
従業員株式購入制度 財形貯蓄制度 親睦や余暇への補助
旅行/パーティー補助金/クラブ活動に対する援助
余暇施設、宿泊施設・レジャー施設などの割引制度、保養施設利用補助""
給与改定: 毎年4月
賞与支給: 毎年3月
加入保険: 健康保険  厚生年金保険  労災保険  雇用保険


【応募条件】
Qualifications
Education/Experience Required:
Undergraduate degree in science or pharmacology is a MUST.
MD, PharmD or MSc degree in scientific related discipline is preferred.
Previous experience as MSL in Ophthalmology is preferred.
Demonstrated Pharmaceutical industry experience in Medical Affairs, Clinical Development, Safety reporting or research will also be considered.
Ability to comprehensively learn new subject areas and environments.
Keen interest in developing and maintaining expert knowledge for assigned therapeutic area/product and medical research in general.
Key in-Field Team (IFT) Competencies:

Ability to understand the unmet needs of key stakeholders, make decisions that have an impact and execute the integration and assimilation of that information into the IFTs’ engagement approach.
Ability to coordinate scientific/medical engagement efforts across stakeholders within a single account in order to develop interaction plans that are in-line with the Scientific Interaction Plan (SIP) to achieve medical objectives.
Effectively communicate, collaborate and incorporate the views of other in-field team members to optimize business objectives.
Collaborate as needed with Clinical Development in-field teams for acceleration of patient enrollment in clinical studies designated as enterprise critical through scientific engagement with Principal Investigators.

Essential Skills & Abilities:
Proficient with Microsoft Office Suite (Outlook, PowerPoint, Excel, Word, etc.)
Must be at ease with technology (the use of various tools/systems to perform day-to-day tasks).
Excellent written and spoken communication and presentation skills in Japanese, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians and other healthcare decision makers.
High proficiency in English reading, writing and speaking skills is preferred.
This function is typically field based with up to 20% of an individual’s working time spent in the office and remaining 80% in the field.
Drive results through high customer oriented mindset

この求人に問合せる無料

電話からのお問い合わせ

0120-337-613

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受付時間:9:00〜18:00(平日)

関連する常勤求人

2026年10月05日更新

300426599

  • 当直なし
  • オンコールなし

【東京都】MD求人

勤務地
東京都内
給与
1500万円 応相談
募集科目
製薬会社
勤務内容
その他
We are expanding our Field Medical Affairs team to bring innovative solutions in oncology and hematology oncology to the forefront. As a Senior Manager, Field Medical Affairs, you will play a pivotal role in advancing scientific exchange, collaborating with therapeutic area experts, and supporting clinical development initiatives. Join us in shaping the future of healthcare while contributing to meaningful, impactful work in a dynamic and collaborative environment.

A Typical Day:
As part of your role, you will:
Identify and maintain relationships with medical and therapeutic area experts, investigators, and other stakeholders.

Respond to scientific and clinical inquiries in compliance with industry regulations.

Perform disease management and therapeutic area education for practitioners, payers, and researchers.

Attend medical conferences to gather and report scientific, clinical, and competitive intelligence.

Collaborate with investigators and internal medical affairs teams to support investigator-initiated studies (IIS).

Assist in the development and communication of clinical data through abstracts, posters, presentations, and manuscripts.

Support site initiation and enrollment activities for clinical trials.

Ensure adherence to company policies, procedures, and compliance standards.

This Role May Be For You If:

You are passionate about oncology and have deep knowledge in lung cancer, solid tumors, or hematology oncology.

You thrive in a collaborative, matrix organization and enjoy building relationships in academic and clinical practice settings.

You have excellent communication skills and are fluent in both Japanese and English.

You are experienced in immuno-oncology and clinical trials, and possess a strong commitment to compliance.

You are comfortable traveling 30–50% of the time to engage with stakeholders and attend conferences.

2026年10月05日更新

300426597

  • 当直なし
  • オンコールなし

【東京都港区】外資系大手製薬メーカー

勤務地
東京都都内
給与
1200万円 応相談
募集科目
製薬会社
勤務内容
その他
Objectives:

The Medical Science Liaisons (MSL) will work cross functionally with several internal stakeholders such as Medical Therapeutic Area Lead, Medical Manager, Medical Advisor, Scientific Advisor and other MSL of the team, Medical Information team, Pharmacovigillance and Drug Safety Evaluation teams, The Brand Manager and Brand Team members to ensure proper relationship is developed, nurtured and ’s scientific credibility is advanced with established and emerging external experts (EEs) in the therapeutic area of headache and migraine. This position is based in Tokyo and will report to the MSL Manager, Parkinson’s Disease.

Key Responsibilities:
Lead the development and maintenance of key scientific evidence and knowledge on products for credible dissemination to external experts and healthcare professionals in the treatment of Parkinson’s Disease.
Lead the identification of properly qualified external experts to engage with as determined by the medical functional plan as well as in collaborative efforts such as Advisory Board meetings, medical educational programs, congress symposia and potential research collaborations.
Lead the scientific support to and relationships with targeted external experts including key academic societies are maintained by delivering on time credible scientific information through individual or in group interactions.
Ensure infield activities are executed with high integrity and in accordance with the medical functional plan, insights collected through scientific engagement with targeted external experts are summarized, shared as needed with the Brand Team members and other internal stakeholders including Area/Global Medical team and integrated to support the development and further update of medical functional plan.
Work with local Medical Information as appropriate to ensure responses to the unsolicited scientific requests including off-label information on medicines are accurate, up to date, reviewed and approved by local relevant internal and external procedures.
Act as the point of contact with thought leaders to connect their request for support on investigator-initiated study (IIS) related to products and/or pipeline assets to area/global medical team’s review and further support whenever appropriate.
Adherence to all applicable local and international laws and regulations, guidelines, codes of conduct, standards, policies and procedures.
Attend Parkinson’s Disease related local and international scientific meetings and/or conferences and ensure summaries of key data are developed and further shared among the brand team members.
For countries involved in the 1-7-5 early touchpoint process: ensure scientific insights on the current clinical practices are provided on a timely manner into the future clinical development program for pipeline assets.
Pursue as committed the one team cross-functional in-field collaboration with commercial teams and other internal stakeholders as needed to achieve the Brand Team business objectives
Upon request, lead the proper support to prescribers with requests for access to medicines on a named patient or compassionate use basis (subject to all applicable legal and regulatory requirements).
Ensure all mandatory trainings are attended and properly documented.

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  • 高額求人特集2,000万円以上可能!大幅な年収アップも可能
  • 管理職求人特集 キャリアアップ転職に最適
  • 医療機関求人特集 将来の開業に向けた支援がある
  • 福利厚生が充実している医療機関求人特集

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