Regeneron Pharmaceuticals, Inc (USA) Posted October 1, 2026

Sr Scientific Writing Specialist

Remote, United States Full time
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Regeneron Pharmaceuticals, Inc (USA) is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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]

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

This role requires:

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: experience using digital technology-based solutions (e.g., AI, PerfectIt) to streamline content creation or workflows

Preferred: basic understanding of the eCTD and drug development process

Preferred: strong background in protein therapeutics and/or gene therapy

A cover letter is strongly encouraged.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. 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.  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.  If you have any questions, please speak with your recruiter.

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. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

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

Job details

Seniority
Senior
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Remote, United States
Employment type
Full time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 82 comparable Senior Regulatory Affairs roles across 40 biopharma companies.

82Comparable roles tracked
75Currently active
40Companies hiring similar roles
21Countries represented

Salary context

32 of 82 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $93,900/yr – $153,300/yr
Lowest disclosed · Senior Regulatory Affairs Specialist (OTTAVA) · Johnson & Johnson $92,000/yr – $148,350/yr
Peer group range $120,175 – $245,000 (median $192,938)

Where these roles are based

Top locations among the 82 comparable roles

United States37
India5
China5
United Kingdom5
Japan4
Mexico3

+ 15 more countries

Seniority mix

82 of 82 peers have a known seniority level

Senior39
Associate Director39
Principal4

Therapeutic area mix

5 of 82 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Dermatology & Aesthetics2
Vaccines & Infectious Disease1
Oncology1
Immunology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Amgen Inc. Remote, United States Senior
Same function Same seniority Same country
60%similar
Merck KGaA Milwaukee, Wisconsin, United States Senior
Same function Same seniority Same country
60%similar
Neurocrine Biosciences Inc. US CA San Diego, United States Senior
Same function Same seniority Same country
60%similar
Johnson & Johnson Santa Clara, United States Senior
Same function Same seniority Same country
60%similar
Amgen Inc. Remote, United States Senior
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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Amgen Inc. · Remote, United States · Senior
Function Therapeutic area Seniority Country
60%
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Function Therapeutic area Seniority Country
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Amgen Inc. · Remote, United States · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.