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丁香人才 > 职位招聘 >医药研发/制药生产招聘 >数据管理员招聘 >上海数据管理员招聘 >黄浦区数据管理员招聘 >Medical Writing Specialist / Manager招聘

Medical Writing Specialist / Manager

礼来国际贸易(上海)有限公司 2017-03-30发布 2017-12-12截止
  • 学历要求: 硕士
  • 英语要求: 熟练
  • 年龄要求: 不限
  • 专业要求: 基础医学,临床医...
  • 工作年限: 二年以上
  • 月薪范围: 面议
  • 职位性质: 全职
  • 工作地点: 上海市黄浦区
  • 职称要求: 不限
  • 招聘人数: 2人

职位描述

Position Title: Medical Writing Specialist / Manager

Location: Shanghai

Purpose:
The Specialist, supporting Asia-Pacific Medical Communications (APMC)China, is responsible for proactive customer and vendor interaction andperforms as a partner to accomplish the objectives of the medicalcommunications team. This requires a clear understanding of the teamstrategy and the activities necessary to meet team goals such asworkflow management and document assignments. Additionally, theSpecialist will proactively lead and project manage outsourcedscientific documents or materials (eg, right to operate regulatorydocuments, slide kits). The Specialist also establishes appropriatebusiness relationships and acts as a single point of contact for vendorsand customers of the medical communications team.
Primary customers include but are not limited to APMC, Medical, Safety,Regulatory, Marketing, Legal, Clinical Pharmacology, and externalcustomers such as Investigators, Opinion Leaders, and vendors worldwide.
Responsibilities:
1. Scientific Communications Support (30%) • Use creativity tointroducing new tools, processes, and structure to accomplish broaderorganizational goals and meet standards while providing solutions tostreamline team workflow.
• Improve document processes by establishing uniformcross-organizational practices; suggest process or tool enhancements toimprove effectiveness and minimize redundancy between databases andother tools.
• Serve as a resource for others associated with documentprocess/products and be an expert on specifications, timelines, andprocess.
2. Scientific Communications Document Development (35%)
• Provide direct editorial and project management support, and/oroversee vendors to support, the planning, editing, and timely submissionof scientific documents including: formatting, proofreading, andconducting literature searches, working with the writing team toestablish and track key milestone timelines; editing documents forstyle/usage and content; obtaining and processing copyright transfer andauthorship agreements; verifying data and references for accuracy;creating figures and diagrams, writing cover letters to journal editorsand submitting manuscripts, and coordinating and/or conductingtranslation validation.
• Own the processes for document submission along with all associatedfinal steps in the submission of publications and the delivery ofregulatory documents to the regulatory function, acting as a singlepoint of contact for regulatory operations and publishing groups.
• Accountable for achieving timelines by managing support activitiesefficiently and proactively; utilize ability to understand and applyteam communication strategies to work products.
• Ensure poster and presentation materials are present at scientificmeetings; own finalization steps for submission to scientific meetingsand journals.
• Responsible for the end-to-end creation of materials using varioussoftware programs such as Excel, PowerPoint, Sigma Plot, and internalsystems such as Leo, Libra, Datavision, and LillyNet (SharePoint).
• Coach new Medical Communication Specialists or others requiringdevelopment in core areas.
3. Database Management & Maintenance (35%)
• Track document metrics across groups as assigned by the supervisor(e.g., budget, documents completed, publication plans and outcomes).
• Manage Datavision, including performing data steward responsibilities.
• Manage logistics for Business and Scientific Disclosure Planning,including current and emerging technologies impacting businessprocesses.

Minimum Qualification Requirements:
 Master degree in Medial Science equivalent, overseas educationexperience preferred.
 Strong communication skills in English and local language(s),including written and verbal communication (including IELTS[International English Language Test System], TOEFL [Test of English asa Foreign Language], and/or TOEIC [Test of English for InternationalCommunication] scores if available).
 Demonstrated ability to communicate and negotiate solutions to complextechnical challenges with cross-functional colleagues, external vendorsand customers.
 Demonstrated project management and time management skills.
 Cognitive abilities, including verbal reasoning, attention to detail,critical thinking, and analytical ability.
 Interpersonal skills and the ability to be flexible in varyingenvironments.
 Ability to utilize high-level end-user computer skills (e.g., wordprocessing, tables and graphics, spreadsheets, presentations andtemplates).
 Ability to work well independently and as part of a team, within andacross culturally and geographically diverse environments.
 Proven ability to assemble, share and apply key learnings acrossmultiple projects
Other Information/Additional Preferences:
 Specialized knowledge of editing & proofreading techniques.
 Limited travel, up to approximately 10%.

联系人: 盛烨

地    址:上海市静安区石门一路288号兴业太古汇香港兴业中心一座第16-19层

美国礼来制药(Eli Lilly andCompany)是一家全球性的以研发为基础的医药公司,创立于1876年,总部位于美国印地安那州印第安纳波利斯市,业务遍及全球 125个国家和地区。礼来致力于为全人类提供以药物为基础的创新医疗保健方案,使人们生活得更长久、更健康、更有活力。

礼来制药与中国的渊源可以追溯到二十世纪初页。礼来于1918年来到中国,并将其第一个海外代表处设在上海,从而迈出了全球化的第一步。几经风雨历练,礼来于1993年重返中国。二十年多来,礼来本着“植根中国,造福中国”的理念,着力拓展在华业务,目前已经形成从研发、生产到商业运营的全产业链 ...详情

单位概况

礼来国际贸易(上海)有限公司
近两周应聘简历处理率:48%
制药/生物工程
医药企业 其他
1000~9999人
上海市静安区石门一路288号兴业太古汇香港兴业中心一座第16-19层
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