医学撰写员
Medical Writer
职位名称：医学撰写员
工作地点：印度远程办公
工作地点类型：远程
工作合同类型：全职
职位级别：
工作时间安排
标准（周一至周五）环境条件
办公室职位描述
加入我们，成为医学撰写员——在创新前沿发挥作用
医学撰写员从规划和协调到最终稿件的交付，为内部和外部客户提供高质量的医学和科学写作。该职位涉及与内部和外部客户合作，支持并促进有效的沟通，从而实现运营卓越。
您将负责：
• 作为主要作者撰写并提供对常规文件（如临床研究报告和研究方案）的输入，并总结临床研究的数据。
• 可能协助撰写更复杂的临床和科学及项目级文件，包括IB、IND和MMA。
• 确保所负责文件符合质量流程和要求。可能协助确定实现最佳结果的最佳实践、方法和技术。
• 可能协助进行项目管理活动。职责可能包括协助制定所负责交付物的时间表、预算和预测。
• 在项目启动会议、评审会议和项目团队会议上代表部门。
教育与经验要求：
• 科学学科的学士学位或同等学历及相关正式学术/职业资格
• 具备履行该职位所需知识、技能和能力的先前经验（相当于3年以上）
• 在制药/CRO行业的工作经验优先
• 科学写作经验有优势
工作经验年限是指获得履行该职位必要知识、技能和能力通常所需的年限。工作经验不应作为确定职位等级或做出雇佣决策的唯一依据。
知识、技能、能力：
• 扎实的医学写作能力，包括语法、编辑和校对能力
• 能够准确且简洁地解释和呈现复杂数据
• 有效的行政、组织和计划能力；注重细节和质量
• 能够独立工作并在团队中有效协作
• 有效的口头和书面沟通能力
• 良好的知识
查看英文原文
Job Title: Medical Writer
Job Location: Remote, India
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Join Us as a Medical Writer - Make an Impact at the Forefront of Innovation
The Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. The role involves collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.
What You'll Do:
• Serve as primary author who writes and provides input on routine documents such as clinical study reports and study protocols and summarizes data from clinical studies.
• May assist with more complex clinical and scientific and program level documents, including IBs, INDs, and MAAs.
• Ensure compliance with quality processes and requirements for assigned documents. May assist in determining best practices, methods and techniques for achieving optimal results.
• May assist in program management activities. Duties could include assisting with developing timelines, budgets, and forecasts for assigned deliverables.
• Represent the department at project launch meetings, review meetings, and project team meetings.
Education & Experience Requirements:
• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years).
• Experience working in the pharmaceutical/CRO industry preferred
• Experience in scientific writing advantageous
Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
Knowledge, Skills, Abilities:
• Solid medical writing skills, including grammatical, editorial, and proofreading skills
• Ability to interpret and present complex data accurately and concisely
• Effective administrative, organizational and planning skills; attention to detail and quality
• Ability to work on own initiative and effectively within a team
• Effective oral and written communication skills
• Good knowledge of regulatory documentation and drug development process
• Great judgment and decision-making skills
• Good computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)
Working Conditions and Environment:
- Exposure to electrical office equipment.
- • Occasional drives to site locations with occasional travel both domestic and international.
- • Long, varied hours required occasionally.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.
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Originally posted on Himalayas