Regeneron is looking for a Scientific Writer to join our team. In this role, you will be responsible for drafting and managing reviews of submission documents for nonclinical pharmacology across therapeutic areas. You will work directly with scientists to interpret data, develop key messaging, and prepare content for global health authority submissions.
What You'll Do
- Work with scientists, Research Program Management, and Regulatory Affairs to interpret and develop the data package for a drug candidate.
- Independently author and manage internal reviews of nonclinical study reports, eCTD summary documents, and Investigator’s Brochures.
- Drive documents through comment reconciliation by creating consensus among key stakeholders up through Senior Management.
- Simultaneously advance multiple projects while adhering to submission target timelines.
- Participate in process improvement by creating or revising internal guidance documents and templates, or by implementing new technology solutions.
- Train and support consultants or junior writers working within the Scientific Writing group.
What We're Looking For
- BS or MS with 6+ years, or PhD in a Life Sciences-related field with 2+ years of relevant experience (e.g., scientific/regulatory writing or pharmaceutical industry).
- Experience with the eCTD and the drug development process.
- Strong attention to detail, time-management skills, and scientific rigor.
- Computer proficiency (Word, Excel, Adobe, GraphPad Prism).
- Fluent in the English language.
Technical Stack
- Word
- Excel
- Adobe
- GraphPad Prism
Team & Environment
You will work within the Scientific Writing group.
Benefits & Compensation
- Salary range: $108,300.00 - $176,700.00
- Health and wellness programs
- Fitness centers
- Equity awards
- Annual bonuses
- Paid time off
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.
