Sr Scientific Writing Specialist

Regeneron Pharmaceuticals, Inc (USA); United States; Remote; USD 94,000 - 153,000; Full time

Benefits offered by this job

Annual bonuses

Equity awards

401(k) company match

Health and wellness programs

Pension or retirement benefits

Paid time off

Family support benefits

Fitness centers

Insurance benefits (medical, dental, 视

Job summary

Regeneron Pharmaceuticals, Inc. seeks a Sr. Scientific Writing Specialist to draft and manage reviews for Clinical Bioanalysis and Clinical Pharmacology submission documents across multiple therapeutic areas and clinical phases.

You will lead document meetings, coordinate timelines, and collaborate with cross-functional teams to streamline content development. The role emphasizes strong attention to detail, excellent communication, and proficiency in Word, Excel, and Adobe within an on-site US

Qualifications

• BS degree with 2+ years of relevant experience or MS/PhD/PharmD in life science.
• 1-2 years of relevant industry experience in biotech/pharma setting.
• Excellent interpersonal and written communication skills.

Responsibilities

• Draft and manage reviews of reports and summaries for Clinical Pharmacology and Clinical Bioanalysis.
• Lead Kickoff, Author, and Comment Reconciliation meetings for assigned documents.
• Attend cross-functional program meetings and report relevant strategic information to the writing team.
• Manage multiple projects and timelines.
• Review data outputs for consistency with stylistic standards.
• Maintain and revise document templates or shells.

Skills

Scientific writing

Cross-functional collaboration

Attention to detail

English communication

Word/Excel/Adobe

Education

BS degree with 2+ years

MS/PhD/PharmD in life science

Tools

Word

Excel

Adobe

Job description

About the Role

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. 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. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where: Location: [Insert location] Work model/flexibility: [Insert work model]

Key Responsibilities

• Discover your role: Independently draft and manage review of reports and summaries for the Clinical Pharmacology and Clinical Bioanalysis functional areas
• Lead Kickoff, Author, and Comment Reconciliation meetings for assigned documents
• Attend cross-functional program meetings and report relevant strategic information back to the writing team and management
• Manage multiple projects and timelines
• Review data outputs for consistency with stylistic standards
• Participate in the revision and maintenance of document templates or shells
• Bring strong attention to detail and excellent interpersonal and communication skills
• Stay curious about digital technology-based solutions that streamline content creation and daily workflows

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
• Strong attention to detail
• Excellent interpersonal and communication skills (verbal and written)
• Computer proficiency (Word, Excel, Adobe, and related software) and fluency in English

Preferred Qualifications

• 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
• Strong background in protein therapeutics and/or gene therapy

We are committed to building a workplace with an inclusive culture.

Equal Opportunity Employer

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, sexual orientation, gender identity or expression, gender reassignment, 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, genetic information, military or veteran status, or any other characteristic protected under applicable law.

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.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.

Benefits

• annual bonuses or other incentive plans
• equity awards
• pension or retirement benefits
• 401(k) company match
• health and wellness programs
• fitness centers
• insurance benefits (e.g. medical, dental, vision, life and disability)
• paid time off
• family support benefits

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits.

For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/.

For other locations, additional information will be provided during the recruitment process.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site.

Background Checks

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. 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.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$93,900.00 - $153,300.00

About Regeneron

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA-approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases. Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company's Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.