• 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06月12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。
・時間外労働:あり
・加入保険
  社会保険:健康保険、厚生年金保険
  労働保険:雇用保険、労働者災害補償保険

【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06月12日更新

300425364

  • 当直なし
  • オンコールなし

【東京・大阪】MD求人

勤務地
東京都東京・大阪
給与
1400万円 ~ 2300万円 応相談
募集科目
製薬会社
勤務内容
その他
Project Physician (PP) is a medical expert who is accountable/responsible for generating clinical development strategy, designing clinical development options, and delivering successful clinical development programs for assets in Japan.
His/Her accountability/responsibility is mainly at project-level, however, he/she is also involved in study-level activities as needed.

Other major responsibilities/accountabilities include but are not limited to:

Generate Japan clinical development strategy in collaboration with Clinical Scientist (CS) by providing expert knowledge as a physician-scientist, influencing the study design such that it reflects clinical practice, evolving landscape of medicine, regulatory and reimbursement requirements and that it meets the strategic program objectives.
Draft and/or review study design, regulatory documents to ensure alignment with agreed clinical development strategy.
Be responsible/accountable for KEE engagement from R&D perspectives including but not limited to group advisory board mtg and 1:1 consultation as local internal medical expert to lead scientific discussion for clinical development strategy in collaboration with CS and global teams.
Act as a study physician of Japan standalone studies as well as support global study physicians of global leading studies
For more information about responsibilities/accountabilities, refer to the full version of the Job Description for Project Physician

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医師求人特集

  • 週4日の勤務可能の常勤 生活の質を重視する意思に評判!
  • 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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