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As a key individual contributor part of a R&D team to drive the functional ingredients innovation by cooperating with external partners.
You will lead a project team and be responsible for the medical device business landing and launching program in China market from regulatory, safety, claims aspects.
The China Regulatory Affairs Manager will provide leadership and strategic direction for the Regulatory department in China. They will ensure that all local regulatory requirements are met throughout product lifecyle, from guiding formula development and innovation, to reviewing marketing/advertising materials such as labels and securing advertising permits, to handling post-launch reporting.
Est.1981, mature enterprise who delicate into the bee product head down;Servicing domestic and international clients with various products covering food&beverage, personal care, health & nutrition, animal care, and different types of OEM/ODM depending on requests
Full cycle Regulatory Affairs support from plant to end product;Provide RA advice for NPD;Cross function prepare related documents including but not limited to labels and raw material list;
As the Head of Biometrics, the person is expected to serve as the biostatistics expert who will manage external partners for biometric work across all sites in China, and further develop internal team to perform all statistical work of clinical studies conducted by the company; provide sound experimental design and data analysis expertise; prepare statistical analysis plan to ensure that the appropriate statistical methods are developed and utilized; interface with other functions and global teams to assist with data interpretation and understanding of results.
As a Chief Science Officer you will be responsible for science strategy and building research capability including team and laboratory. You will be responsible for overseeing the development of the company's mission and strategic objectives by advancing assets through pre-clinical and early clinical development.
我们正在寻找一位有经验的生物主管加入一家生物技术公司.
流式及成像技术支持
负责公司油脂类产品业务相关的法规事务,产品注册,内外部法规支持。
Head of Global Communications roles is central to our Client's long-term strategy in China and Global. You will work together with C-Level leadership team to formulate internal and external communications strategy. This will be driven by thought leadership and centred around progress with Pre-Clinical and Clinical assets.
Our client is seeking Pre-Clinical Head-Oncology to provide strategic scientific leadership in both discovery and early clinical development programs. This position reports directly to the CEO of the company and work closely with Scientific Advisory board and other relevant functions.You will also take responsibility to establish and run Innovation Research Centre in Pudong, Shanghai.
Support Head to develop and engage internal talents Work as an internal consultant, to provide professional guidance on specific training needs, training structure and training course development. Mainly responsible for leadership training for commercial team, and be in charge of capability assessment work.
Supporting clinical development activities in all therapy areas, driving the progress and acceleration of innovative assets into the market.
It will involve quality control review of study related documents, study monitoring as it relates to cruelty free studies as well as the creation/revision/review of standard operating procedure SOPs, timely completion of deviations and investigations, and implementation and periodic review to ensure compliance to applicable FDA/health authority regulations and ICH (International Council for Harmonisation), Good Clinical Practice (GCP) guidelines and SOPs.
This role with report to CEO of the company and lead all Clinical Operations activities related to the current oncology pipelines. You will play crucial role in forming Clinical Operation capability internally at the same time assuring the progress of existing trials.
You will oversee Clinical Operations for Oncology Therapeutic area in APAC region focusing on strategic and operational activities related to Phase I to Phase III stage clinical programs.
This is a comprehensive role of portfolio strategy for a renowned multinational pharmaceutical company. This role will be fully responsible for establishing and executing strategy to scout and develop a portfolio of innovations that are aligned with the organisational strategic priorities
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