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无工作经验 -
招1人 -
11-09 发布
- 五险一金
- 补充医疗保险
- 补充公积金
- 员工旅游
- 通讯补贴
- 专业培训
- 绩效奖金
- 年终奖金
- 弹性工作
- 定期体检
职位描述
职位描述： Job Overview:The Medical and Regulatory Writer works under the supervision of a more experienced medical writer or with minimal supervision on the preparation of clinical and regulatory documents for a wide range of therapeutic areas, performing the tasks listed below.职责描述：Job Duties and Responsibilities:?Write, edit, format, compile and review assigned documents requested by internal cross-functional teams and/or clients?Coordinate overall quality review of documents?Perform quality checks for internal consistency of data, compliance with applicable templates and style guides, accuracy and completeness of references, etc.?Ensure delivery of requested documents according to timelines within budget and to acceptable quality standards?Provide support to other medical and regulatory writers to ensure delivery of documents according to timelines and within budget and to acceptable quality standards?Participate in training activities to expand medical and regulatory writing capabilities (e.g. writing expertise, different kinds of documents, understanding clinical and regulatory functions, etc.)?Any other activites related to the position as required by direct supervisor任职要求：oA university degree in the field of science or medicine, graduate/postgraduate degree preferredoScientific/technical writing or publishing experience, CRO experience a plusSkills/CompetenciesoStrong written and verbal communication skills in EnglishoStrong computer skills, including Microsoft OfficeoProficiency in scientific terminology, medical terminology preferredoAble to exercise judgment within defined procedures and practices and to determine appropriate action independentlyoStrong attention to detailoStrong problem-solving skillsoAble to follow applicable local and national regulatory guidance and document specifications with minimum supervision 职能类别： 医药技术研发人员 关键字： medical writer 医学编辑
联系方式
上海
公司信息
In Jan 2014,Choice Pharma(丘以思(上海)医药信息咨询有限公司) merged with Clinipace Worldwide. Clinipace Worldwide is a global full-service digital contract research organization (dCRO) that has pioneered an innovative service model to transform drug and medical device development by delivering technology-amplified services to improve study performance, collaboration, and transparency across all stakeholders. From managing your entire development program to conducting an individual clinical trial, our experts bring extensive therapeutic and local experience in building a well-defined clinical plan to maximize your success. Powered by TEMPO? – our proprietary eClinicaltechnology – our teams ensure your success and bring unsurpassed efficiency, quality, and visibility to your development programs. Now Clinipace Worldwide ranks the 10th CRO,and developes rapidly. Clinipace Worldwide，一个基于科技的全球性全方位服务的数字化合同研究组织（dCRO）。我们开创性的开发了依靠技术创新的CRO服务模式，以满足风险投资支持的，中型的战略性制药，生物技术公司以及医疗器械公司的研发需求。 借助于我们专有的TEMPO?电子化临床试验平台，我们的专家团队用他们丰富的治疗领域知识和见解来帮助生命科学公司制定和执行注册策略，临床开发和上市后研究，以确保药物和医疗器械开发计划的成功。 Clinipace Worldwide的唯一目标就是通过开拓创新的技术继续坚定不移地致力于客户的成功，以最具性价比的全球性解决方案服务客户，提供高透明度，灵活和高质量的服务。 我们已经开展了超过1500个全球性的临床研究，完成了超过300个注册和开发策略制定项目。治疗领域涵盖如心血管和代谢，中枢神经系统，皮肤，消化，免疫，感染，肾脏，肿瘤，呼吸，风湿和疫苗（和其他细胞和组织疗法）。 Clinipace Worldwide刚刚庆祝了他们的10週年。如今，Clinipace Worldwide其总部设在美国北卡罗莱纳州的Research Triangle Park，为横跨4大洲的27个国家提供服务。 因为对更高的数据准确度，经济高效的解决方案和更低的研发成本的需求在不断的增加，Clinipace Worldwide还在持续的在全球扩张。 https://www.clinipace.com 最后, 丘以思以正直透明、追求卓越绩效的企业文化邀请您的加入. 应聘邮箱：mwang@clinipace.com
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