掲載期間:22/05/06~22/11/05 求人管理No.019068

外資製薬メーカー

Rare Disease MSL

  • 大企業
  • 年間休日120日以上
  • フレックス勤務
  • 産休・育休取得実績あり
  • 転勤なし
  • 社宅・住宅手当有
  • 退職金制度有
  • 英語を活かす

募集要項

外資製薬メーカーにてMSLとして従事していただきます。

仕事内容

The Medical Science Liaison (MSL) is a Medical Affairs professional who serves as a key scientific partner to
healthcare providers and decision-makers, medical professional associations, and internal colleagues,
in particular those in the assigned Ecosystem(s). He/she engages in peer-to-peer scientific exchanges
relative to the assigned therapeutic area with the asset(s) throughout the product’s life cycle and
gathers/shares crucial insights which can inform business strategies and product development. This
professional will be responsible for planning and implementing key medical strategies to enhance and
positively impact patient care, access and outcomes. The MSL reports to the Head of Medical Science or
MSL Group Lead and is the local medical & scientific expert in the assigned Ecosystem(s).

MAJOR ACCOUNTABILITIES
External Stakeholder Engagement
・Develop/manage external stakeholders including KOL identification, effective KOL engagement, and efficient territory management
・Develop, execute and maintain individual Medical Plan for key KOLs in line with Area Medical Plan objectives
・Manage territory effectively with approximately 70-80% of time focused on external stakeholder interactions (area dependent)
o Strong stakeholder engagement through collecting/sharing of KOL insights, tailoring of scientific proposal to KOL needs and alignment of scientific partnership for delivery of value for the KOL/HCP and the patients/caregivers
・Collect, analyze, and communicate information concerning therapeutic area, treatment options, emerging standards of care, and competitive intelligence
・Scientific support of external experts in the context of sharing new and relevant data,advisory boards, congresses, medical education or publications
・Support market access from a scientific perspective through scientific exchanges with hospital pharmacists and others
・Support clinical trials, non-interventional and other RWE studies through the collection and communication of medical and scientific knowledge when requested or assigned
・Support study management in collaboration and agreement with Development Team Japan and gather and share Medical Insights as necessary
・Facilitate the process of unsolicited Investigator-Initiated Studies (IISs), serving as the main contact person between and the investigator from the investigator request to the publication
Functional Expertise
・Maintain and leverage strong and up to date therapeutic expertise (scientific, clinical, disease states, and treatment alternatives knowledge within the therapeutic area(s)) to, in the context of patient’s journey, support tactical execution of territory plan in line with key medical strategies
・Multiple Sclerosis(MS) and/or Optic Neuromyelitis (NMO SD) experiene is (are) strongly preffered
・Demonstrate medical leadership by contributing to key medical and scientific conferences, advisory boards, and clinical investigator meetings upon request by Development Team   Japan
Cross-functional collaboration
・Collaborate and communicate cross-functionally with Ecosystem team to transform HCP insights into actions to deliver superior and sustainable HCP value and impact
・Contribute and share accountability on creation and implementation of the Ecosystem priorities
・Understand and engage with a wide range of stakeholders; proactively collaborate and network with internal partners regionally and shares insights/best practices across the team
・Provision of scientific updates to their peers
・Ensure completion of CRM related documentation/reporting duties, planning duties and timely reporting of insights in line with guidance communicated by Head of Medical Science or MSL Group Lead

COMPLIANCE
・Operate according to standards (policy, processes, guidance) and local regulation (regulatory,
pharma codes, …)
・Apply the highest level of professional standards: Adhere to compliant behavior demonstrated by embracing ethical decision-making practices and guidelines in all aspects of the job.
・Address medical information inquiries and report safety relevant infor mation in a high quality and timely manner according to processes and requirements.

応募条件
【必須事項】
・ Superior scientific profile preferred (MD, PhD in Natural Sciences,
PharmD)
・ 3+ years of MSL experience strongly preferred
・ Relevant therapeutic and clinical experience is a plus
・ Basic understanding of the pharmaceutical industry and
healthcare arena
・ Customer service and patient oriented attitude
・ Willingness to travel extensively, both nationally and internationally
【歓迎経験】
【免許・資格】
【勤務開始日】
応相談
学歴
大学院修士以上
雇用形態
正社員
試用期間
3ヶ月

契約期間
勤務地
東京
転勤の有無
転勤なし
受動喫煙防止措置
敷地内禁煙(喫煙場所なし)
勤務時間
フレックスタイム制 (コアタイム無し、所定労働 7時間30分)
休憩時間
60分
時間外労働
勤務開始日
応相談
休日休暇
週休2日制(土・日)
祝日・夏季休暇・年末年始休暇・有給休暇・慶弔休暇・特別休暇
年収・給与
経験により応相談
諸手当
通勤手当・交替勤務手当・残業手当
昇給
成果に応じて昇給有/年1回
賞与
成果に応じて賞与有/年1回
採用人数
1名 
待遇・福利厚生
【待遇】
退職年金・団体生命保険・長期所得補償保険・定期健診・各種社会保険・財形財蓄制度・育児支援・永年勤続表彰・クラブ活動・英語学習補助・リゾートトラスト施設利用
【福利厚生】
選考プロセス
1)書類選考
2)一次面接
3)二次面接
4)最終面接

外資製薬メーカー

Rare Disease MSL

  • 大企業
  • 年間休日120日以上
  • フレックス勤務
  • 産休・育休取得実績あり
  • 転勤なし
  • 社宅・住宅手当有
  • 退職金制度有
  • 英語を活かす

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