387900BR
Feb 01, 2024
Japan
About the Role
私たちは，革新的な治療法の発見と開発に関わり，より多くの患者さんに新しい方法で治療をお届けするため日々取り組んでいます。そのような画期的新薬の開発において，非臨床薬理担当者の役割は非常に重要であり，候補化合物の開発に携わることで以下のようなやりがいを感じることができます。
Job Purpose:
Promotes the project as a specialist in pharmacology. Specifically, J-NDA, profiling of new compounds/modalities, and contribution to clinical studies in Japan.
Major Accountabilities:
• Work independently and collaborate with cross-functional project teams as a pharmacologist.
• Perform all duties related to the pharmacology field in the (s)NDA (preparation of CTD, HA interaction, etc.)
• Assessment of pharmacological profiles to contribute to Japan development strategy.
• Support clinical studies as a pharmacologist including preparation of protocol/ICF/IB and interaction with HAs.
• Contribute to maximizing the value of the project (proposal of new indications etc.).
• Quality management responsibility
・Ensure adequate reporting of adverse events / technical complaint / compliance issue in accordance with company procedures.
・100% timely delivery of all training requirements including compliance.
Job Purpose:
Promotes the project as a specialist in pharmacology. Specifically, J-NDA, profiling of new compounds/modalities, and contribution to clinical studies in Japan.
Major Accountabilities:
• Work independently and collaborate with cross-functional project teams as a pharmacologist.
• Perform all duties related to the pharmacology field in the (s)NDA (preparation of CTD, HA interaction, etc.)
• Assessment of pharmacological profiles to contribute to Japan development strategy.
• Support clinical studies as a pharmacologist including preparation of protocol/ICF/IB and interaction with HAs.
• Contribute to maximizing the value of the project (proposal of new indications etc.).
• Quality management responsibility
・Ensure adequate reporting of adverse events / technical complaint / compliance issue in accordance with company procedures.
・100% timely delivery of all training requirements including compliance.
Diversity & Inclusion / EEO
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Role Requirements
Education:
MSc or PhD in life sciences (Pharmacology, Biochemistry, other specific sciences), DVM/MD or equivalent professional experience.
Experience/Professional requirement:
• Taking education or possessing knowledge of basic medicine, such as physiology, pharmacology, molecular biology, etc.
• Experience of NDA as a preclinical pharmacologist.
• Proven record as team player with superior communication skills.
• At least 3 years of experience in basic research at a research laboratory of a pharmaceutical company.
• Experience in writing articles in English is preferred.
English Skill:
Appropriate skills of English (read/write and oral)
MSc or PhD in life sciences (Pharmacology, Biochemistry, other specific sciences), DVM/MD or equivalent professional experience.
Experience/Professional requirement:
• Taking education or possessing knowledge of basic medicine, such as physiology, pharmacology, molecular biology, etc.
• Experience of NDA as a preclinical pharmacologist.
• Proven record as team player with superior communication skills.
• At least 3 years of experience in basic research at a research laboratory of a pharmaceutical company.
• Experience in writing articles in English is preferred.
English Skill:
Appropriate skills of English (read/write and oral)
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
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Biomedical Research
Translational Medicine
Japan
Tokyo
Novartis Pharma K.K.
Research & Development
Full Time
Regular
No
