Principal Medical Writer

🔥 2 hours ago

🇮🇳 India – Remote

⏰ Full Time

🔴 Lead

🏥📝 Medical Writer

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Research, write, and edit routine documents including clinical study reports and study protocols • Summarize data from clinical studies • Assist with complex clinical, scientific, and program-level documents, including IBs, INDs, and MAAs • Ensure compliance with quality processes and requirements for assigned documents • Assist with program management activities, including developing timelines, budgets, and forecasts • Participate in project launch meetings, review meetings, and project team meetings • Collaborate with internal and external clients to support effective and efficient communication • Deliver high-quality medical and scientific writing from planning and coordination through final drafts

🎯 Requirements

• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification • Previous experience providing the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years) • Experience working in the pharmaceutical/CRO industry advantageous • Experience in scientific writing advantageous • Basic 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 • Basic knowledge of regulatory documentation and drug development process • Good judgment and decision-making • Competent computer skills and use of templates; basic knowledge of document management systems and relevant applications such as Excel and Outlook • Willingness and ability to occasionally drive to site locations and travel domestically and internationally • Ability to work occasional long, varied hours

🏖️ Benefits

• Fully Remote work arrangement • Standard Monday-Friday work schedule • Collaboration and development opportunities • Global team environment • Occasional international and domestic travel

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