Regeneron
Sr Scientific Writing Specialist
Remote - United States · Senior
Sponsorship not specified$94k-$153kDetected 15 days ago
ExcelPharmacologyCRISPRScientific WritingCommunication
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odds of building a lasting career here
55Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role82
Entry-level history0
PERM / green-card track0
Lottery odds (Level III)83
Fits your clock70
Sponsors, but it's cap-subject — you still face the weighted lottery (~45% per draw at Level III). Good if you win; have a cap-exempt backup on your list.
Lottery odds assume a STEM candidate.
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About the role
- Attend cross-functional program meetings and report relevant strategic information back to the writing team and management
- Review data outputs for consistency with stylistic standards
Responsibilities
- Build our future together:
- Scientific Writing Specialist to draft and manage reviews for Clinical Bioanalysis and Clinical Pharmacology submission documents across multiple therapeutic target areas (Cardiovascular & Metabolism, Oncology, General Medicine, Immunology & Inflammation, Genetic Medicine) and all phases of clinical development (Phase 1 through Phase 3).
- In this role, you will lead document meetings and timelines while collaborating with cross-functional program teams, with the opportunity to contribute to digital technology-based solutions for content generation.
- Independently draft and manage review of reports and summaries for the Clinical Pharmacology and Clinical Bioanalysis functional areas
- Manage multiple projects and timelines
- We are committed to building a workplace with an inclusive culture.
Requirements
- BS degree with 2+ years of relevant experience, or MS/PhD/PharmD in a life science
- 1-2 years of relevant industry experience in a biotech/pharma setting
- Computer proficiency (Word, Excel, Adobe, and related software) and fluency in English
- For that reason, many roles are required to be performed on‑site.
Nice to have
- experience using digital technology-based solutions (e.g., AI, PerfectIt) to streamline content creation or workflows
- basic understanding of the eCTD and drug development process
Skills
- Bring strong attention to detail and excellent interpersonal and communication skills
Compensation
- Where necessary, we disclose salary ranges for roles in all countries in which we operate.
Benefits
- In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.
- For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/.
- The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
Company info
- Please be advised that at Regeneron, we believe we do our best work when we are together.
- As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based.
- At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases.
- We are seeking a Sr.
Equal opportunity
- Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Visa & Work Authorization
- ignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status
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This listing is sourced directly from Regeneron's careers page and normalized into a canonical job model.