• 招聘类型：社招
• 工作性质：全职

职位描述

• Works effectively with cross-functional groups to produce high-quality, scientifically accurate documents under strict timelines, and ensures consistency between related documents
• Develop and manage timelines and communicate with team members to maintain awareness of expectations, milestones, and deliverables
• Ensure clinical documents adhere to BeiGene standards and regulatory guidelines
• Ensure that assigned documents undergo a quality check before approval, and that documents are routed correctly during review and approval cycles
• Ensure the key messages as defined by the team are clearly and adequately represented in the documents; drive the team to reach agreement in case of conflicting opinions.
• Establish effective cross-functional communication and relationships with counterparts both internally and externally.
• Participate in departmental or interdepartmental process improvement and training initiatives.
• Mentor and manage entry-level FTE writers as needed

任职条件

• Minimum requirement of a master’s degree of life science/pharmacy/ nursing/medical/health related science or equivalent; PhD/PharmD in life sciences preferred
• More than 1 years of relevant industry experience as a regulatory medical writer
• Demonstrated ability to communicate and write English clearly, concisely, and effectively
• Excellent interpersonal skills; a team player
• Ability to coordinate and manage communications to enable timely reviews from other authors and reviewers and to function as a collaborative team member
• Ability to understand and interpret clinical and scientific data; ability to present results in an understandable manner
• Ability to complete high-quality documents according to tight timelines
• Ability to comply with company and/or industry style guides and templates
• Strong project management skills
• Technical expertise in Microsoft Word, Adobe Acrobat, and electronic

职位要求

• 学历要求：无
• 工作经验：无
• 外语要求：不需要

公司福利

• 五险一金 
• 晋升空间 
• 法定节假日