Medical Writer – Global Clinical Development

Job not on LinkedIn

🔥 1 hour ago

🗽 New York – Remote

🗽 New York – Remote

💵 $109.9k - $179.3k / year

⏰ Full Time

🟢 Junior

🏥📝 Medical Writer

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This company has sponsored H1B visas in the past.

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Regeneron

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1988

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

💰 Post-IPO Equity on 2023-10

Healthcare • Manufacturing • Biotechnology

Regeneron is a biotechnology company dedicated to turning scientific discoveries into life-changing medicines. The company focuses on a range of serious diseases including allergic, cardiovascular, and metabolic diseases, neuroscience, oncology, hematology, ophthalmology, and rare diseases. It achieves this by integrating biology and technology to develop cutting-edge biologics and genetic medicines. Regeneron is committed to health equity, environmental sustainability, and supporting future STEM talent through initiatives like the Regeneron Science Talent Search. By maintaining high ethical standards and corporate responsibility, Regeneron aims to push the boundaries of science for better healthcare solutions.

📋 Description

• Develop clinical documents including clinical study reports, protocols, informed consent forms, narratives, and investigator brochures • Manage and facilitate document completion with oversight from Medical Writing leads • Lead document activities for a compound when assigned • Drive document development meetings and support timeline execution • Articulate document strategy and document timelines • Identify appropriate stakeholders for content decisions and keep discussions progressing • Synthesize complex discussions into clear, accurate written content • Collaborate with colleagues and help resolve issues while escalating concerns when needed • Support timely, compliant document delivery across therapeutic areas • Collaborate with cross-functional study teams and Medical Writing colleagues

🎯 Requirements

• Bachelor’s degree; advanced degree preferred • 1 year of relevant experience • Awareness of the clinical research process and applicable regulations and guidelines • Scientific and technical reading, writing, and editing skills • Experience following internal standards, procedures, templates, and peer-review practices • Knowledge of guidelines, templates, and standard operating procedures for Medical Writing documents • Working knowledge of Microsoft Word, Adobe Acrobat, and PowerPoint • Familiarity with electronic document management systems • Strong organizational, interpersonal, and communication skills • Ability to maintain current knowledge of industry standards and complete required training

🏖️ Benefits

• Annual bonuses or other incentive plans • Equity awards • Pension or retirement benefits • 401(k) company match • Health and wellness programs • Fitness centers • Medical, dental, vision, life, and disability insurance benefits • Paid time off • Family support benefits • Reasonable accommodation during the recruitment process where required