职位
Toxicology Study Manager
The position is within the toxicology group in Pharmaceutical Sciences (PS)
and located at China Innovation Center of Roche (CICoR). This group leads in
the development of the non-clinical safety assessment of drug candidates during
the discovery and development phases at Roche.
Your responsibilities are:
* Monitor outsourced Tox studies to ensure study timeline, protocol/report
development, execution and completion of study activities, and timely
communication with internal functional project leaders
* Coordinate and manage test articles/reagent/samples transport process and
related export/import process as applicable to assure the study execution
* Assure outsourcing study scientific integrity and quality, technical
capability and experience, animal welfare, and compliance with GLP and other
regulations as applicable
* Collaborate with global toxicology study manager community and external
partners and provide relevant in vivo/veterinary science input locally where
needed and act as local expert in in vivo/veterinary science
* Manage and update CRO landscaping in Asia and keep current of evolution of
the in vivo/veterinary science
In addition, you are expected to:
* Live the culture of humility, curiosity, and responsibility
* Embrace agile ways of working and collaborative spirit
* Aim for scientific excellence, embrace innovation and utilize emerging
technologies to support risk assessments with continuous learning
* Expand scientific visibility and maintain effective interactions with
internal and external collaborators, and contribute to scientific advancements
in the toxicology field
Profile:
You have a Master or Bachelor’s degree in Veterinary Medicine with >5 years of
working experience in pharma/biotech/CROs. Experience working in GLP regulated
environment. Good knowledge of drug discovery and development, especially
toxicology. Experience working with external CROs preferred. Experience working
in a highly matrixed organization, e.g., cross function colleagues, global
toxicology colleagues, and external CROs. Good organizational and multi-tasking
abilities to simultaneously manage multiple research projects, studies, and
CROs. Good communication skills (English and Chinese).
我们是谁
在罗氏，来自100个国家的100，000名员工不断推动着健康医疗行业的进步。我们一同工作，使罗氏成为了世界领先的以研发为基础的健康医疗集团。我们的成功源于创新、求知和多元化，也源于我们把相互间的差异作为一种优势。为了革新医疗健康领域，罗氏设定了远大的计划，坚持学习和发展，并不断寻找与之志同道合的伙伴。
罗氏提供平等的职业发展机会。