Associate Manager, Scientific Writing

Job not on LinkedIn

🔥 1 minute ago

🇺🇸 United States – Remote

💵 $109.9k - $179.3k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

✏️ Content Writer

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This company has sponsored H1B visas in the past.

👻 Ghost score 0%

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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

• Coordinate authors of regulatory documents from a variety of disciplines within assigned projects • Monitor project timelines and resources, escalating risks to management and supporting timeline negotiations across functional areas • Identify training and development needs of direct reports, providing support and guidance for personnel • Participate in screening and interviewing candidates to satisfy existing and new team needs • Support the creation and maintenance of document templates, SOPs, and working practices • Monitor adherence to document processes, escalating deviations to SW management • Identify areas for process improvement within assigned projects and communicate observations to management • Participate in relevant cross-functional drug development team meetings • Support assignment of deliverables and definition of project priorities under the direction of senior Scientific Writing team members • Coordinate regulatory document authors across disciplines, monitor document quality, and support staff training and professional development

🎯 Requirements

• Bachelor's degree or MS/PhD/PharmD in a life science (advanced degree preferred) • 3-5 years of experience (BS/MS) or 2-3 years (PhD) in the pharmaceutical industry, including at least 3 years in regulatory writing • Ability to manage multiple projects • Excellent organizational, interpersonal, and communication skills • Computer proficiency with Microsoft Office Suite, Adobe Acrobat, and related software • Basic experience with job-relevant AI usage • Fluency in English • Preferred: 1-2 years of experience participating in cross-functional drug development teams • Preferred: previous supervisory experience

🏖️ 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