Medical Writer

🔥 1 hour ago

🇮🇳 India – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥📝 Medical Writer

👻 Ghost score 12%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 Description

• Provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients • Serve as primary author for routine documents such as 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 in determining best practices, methods, and techniques for optimal results • Assist with program management activities, including developing timelines, budgets, and forecasts for assigned deliverables • Represent the department at project launch, review, and project team meetings • Collaborate with internal and external clients to support effective and efficient communication and operational excellence

🎯 Requirements

• Bachelor's degree in a scientific discipline or equivalent relevant formal academic/vocational qualification • 3+ years of previous experience providing the knowledge, skills, and abilities to perform the job • Experience working in the pharmaceutical/CRO industry preferred • Experience in scientific writing advantageous • Solid medical writing, grammatical, editorial, and proofreading skills • Ability to interpret and present complex data accurately and concisely • Effective administrative, organizational, planning, oral, and written communication skills • Attention to detail and quality • Ability to work independently and effectively within a team • Good knowledge of regulatory documentation and the drug development process • Good computer skills and proficiency with client templates, document management systems, Excel, Outlook, and other relevant applications • Great judgment and decision-making skills • Occasional willingness to drive to site locations and travel domestically and internationally • Ability to work long, varied hours occasionally

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule • Collaboration and professional development opportunities • Global team environment • Occasional domestic and international travel

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