位于上海市, c23的 12 个优质senior director, toxicology职位（正在招聘！）

Director, Preclinical Safety (Toxicology) China Head
Novartis —上海市
- 全职
Associate Scientific Director, TB&B
Takeda Pharmaceutical —上海市
6 小时
(Senior) Medical Representative
Bausch + Lomb —上海市
Senior Director, IT Infrastructure, Greater China
Marriott International, Inc —上海市
- 全职
Toxicologist, Senior Specialist
Huntsman —上海市
- 全职
Toxicology Project Leader
Roche —上海市
ExploR&D Translational Medicine
Lilly —上海市
- 全职
Preclinical Pharmacology and External Scientific Operations Lead (Shanghai)
Orum Therapeutics —上海市
- 全职
快速申请
Head, TCO (Translational Clinical Oncology) China
Novartis —上海市
- 全职
(Sr.) Game Designer
Activision —上海市
Early Clinical Development Physician (Oncology)
Novartis —上海市
- 全职
9天
AD/D, Preclinical Development
MSD —上海市徐汇区
- 全职

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Director, Preclinical Safety (Toxicology) China Head

Novartis -
上海市

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职位详情

全职

完整职位描述

Summary

Interact with multi-disciplinary teams during due diligence procedures to critically assess nonclinical safety programs for external drug candidates and provide line function aligned recommendations for follow-up actions

About the Role

Key responsibilities:

Conduct due diligence activities under compressed timelines with the ability to rapidly identify key issues followed by clear and comprehensive communication of risks, issues, gaps and conclusions to the due diligence team.
Lead PCS cross-disciplinary teams as required to further evaluate potential nonclinical safety issues or findings.
Work in close collaboration with the PCS TA Head and Global Head of PCS to ensure that nonclinical safety assessments, mitigation strategies and development plans are fully aligned within the line function
Work in close collaboration with the Translational Medicine External Program (TEP) Team to support further implementation of the TEP model and improve processes and procedures.
Support Biomedical Research Integration Office (BRIO) integration activities
Sought-after mentor and role model for talent development, coaching, and performance discussions across the organization

Key Performance Indicators (Indicate how performance for this role will be measured)

Recognized within Novartis for scientific and regulatory expertise in drug development and safety assessment
Recognized for leadership potential
Extensive experience in nonclinical safety development strategies and evaluation of drug candidates from diverse modalities (including low molecular weight molecules, biologics, oligonucleotides, gene therapy and radionucleotides)
Familiar with R&D disciplines beyond nonclinical safety. Broad knowledge of regulatory guidelines, Quality Management processes and animal welfare requirements relevant for nonclinical safety development programs
Demonstrated ability to communicate scientifically sound nonclinical safety conclusions and mitigation strategies to due diligence, PCS management and Novartis leadership teams

Responsible for authoring the nonclinical safety sections of due diligence assessment reports highlighting key risks, issues, gaps together with potential mitigation strategies and conclusions
Provide PCS development strategy and resourcing requirements in the clinical development plan
Provide input to handover package to specify vendor requirements for transfer of PCS methodologies/data/samples and reports to Novartis after deal signature.
Work closely with BRIO to ensure smooth handover to the assigned PCS PTM and project team during integration of assets
Maintain strict adherence to confidentiality and legal requirements
Mentor colleagues on drug development strategy and project-related matters

Essential Requiremernts:

PhD in pharmacology, toxicology or a related biological science; DVM, PharmD, M.S. or equivalent with appropriate training, a strong biological background or equivalent work experience.
Fluent English
Minimum of 8 years of experience as a full-time nonclinical safety expert in the pharmaceutical industry
Excellent oral and written communication abilities
Able to independently anticipate and analyze issues
Demonstrated ability to manage multiple projects simultaneously

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

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

Division

Biomedical Research

Business Unit

Research

Location

China

Site

Shanghai (Shanghai)

Company / Legal Entity

CN14 (FCRS = CN014) China Novartis Institutes for BioMedical Research Co., Ltd.

Functional Area

Research & Development

Job Type

Full time

Employment Type

Regular

Shift Work

Accessibility and accommodation

Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

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在上海市, c23的senior director, toxicology个职位

Director, Preclinical Safety (Toxicology) China Head

Associate Scientific Director, TB&B

(Senior) Medical Representative

Senior Director, IT Infrastructure, Greater China

Toxicologist, Senior Specialist

Toxicology Project Leader

ExploR&D Translational Medicine

Preclinical Pharmacology and External Scientific Operations Lead (Shanghai)

Head, TCO (Translational Clinical Oncology) China

(Sr.) Game Designer

Early Clinical Development Physician (Oncology)

AD/D, Preclinical Development

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在上海市, c23的senior director, toxicology个职位

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About the Role

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