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Job Information Bristol Myers Squibb Clinical Site Manager in Shanghai China Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines..
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease..
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse..
Major Responsibilities: Take full responsibility to be the Head of BMS China and Hong Kong Regulatory for developing/implementing regulatory strategies, and achieving regulatory submission and approval for new products/ projects..
Job Information Bristol Myers Squibb Clinical Trials Associate in Shanghai China Ability to multiple tasks for 3-5 clinical studies during all phases of protocol execution according to established timelines. Consistently..
Job Information Bristol Myers Squibb IO Senior Medical Rep. in Beijing China At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology,..
Act as PDx Molecular Imaging QA contact in support of PDx Molecular Imaging business China initiatives. Job Description Essential Responsibilities :-responsible for the development and maintenance of the GEHC Quality..
Job Information Bristol Myers Squibb Director, Hematology Clinical Development in Shanghai China Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative..
1.Disseminate and exchange advanced level scientific information as a scientific partner with TLs. Develop and maintain scientific/strategic relationships with External Experts to further understand and gain both insight and/or input..
Major Responsibilities: Assist Regulatory manager for implementing and delivering regulatory submission and approval, and maintenance for new products / projects in assigned therapeutic area within agreed timeline. Ensure regulatory compliance..
Essential Responsibilities:-responsible for the development and maintenance of the GEHC Quality Management System to support the GEHC manufacturing authorization in relation to the oversight of a Contract Manufacturing Organization (CMO)..
Job Description 100% 遵守合规所有的相关规定。 1年以上医、药行业市场营销相关工作经验。 通过 RDPAC 的认证考试。 Locations China Remote Location Worker Type Employee Worker Sub-Type Regular Time Type Full time #LI-Remote Apply Share LinkedIn Facebook Email Xing Explore..
Lead the field medical team in China Develop and Maintain direct contact with External Experts to gather insights and input on treatments, and gain a full understanding of patient needs..