Regeneron Pharmaceuticals, Inc (USA) Posted July 15, 2026

Senior Medical Writer

Remote, United States Full time
Regulatory Affairs Senior

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 Senior Medical Writer to join our Medical Writing team, supporting clinical document delivery across Global Development in a remote work mode. In this role, you will author clinical study reports, protocols, consent forms, narratives, and investigator brochures while collaborating with clinical teams and biostatisticians. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

United States or United Kingdom (remote)

Discover your role:

Author clinical study reports (CSRs), protocols, informed consent forms (ICFs), narratives, investigator brochures, and other regulatory documents across therapeutic areas.

Represent Medical Writing at meetings, drive document development, and articulate strategy and timelines.

Identify the right parties for content decisions and synthesise discussions into clear, accurate prose.

Review work of junior or outsourced writers and CSR-related documents like Statistical Analysis Plans and TFLs.

Write plain-language content such as ICFs and explain complex medical concepts to lay audiences.

Adhere to applicable guidelines, templates, SOPs, and internal training while contributing to process improvement across Medical Writing and Global Development.

You mentor junior staff, manage multiple priorities, and foster collaboration to resolve conflict.

This role requires:

Bachelor's degree required; advanced degree preferred.

Minimum 3 years of medical writing experience, including working knowledge of biostatistics.

Strong knowledge of the clinical research process and applicable regulations, including ICH GCP.

Clinical document reading, writing, and editing experience.

Strong knowledge of MS Word, Adobe Acrobat, PowerPoint, and electronic document management systems.

Ability to manage multiple projects with strong organisational, interpersonal, and communication skills.

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)

$128,600.00 - $210,000.00

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 54 comparable Senior Regulatory Affairs roles across 29 biopharma companies.

54Comparable roles tracked
53Currently active
29Companies hiring similar roles
19Countries represented

Salary context

11 of 54 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 $128,600/yr – $210,000/yr
Highest disclosed · Principal Scientist, Regulatory Liaison · Merck $173,200/yr – $272,600/yr
Peer group range $98,050 – $222,900 (median $205,000)

Where these roles are based

Top locations among the 54 comparable roles

United States19
Ireland7
India6
Poland3
United Kingdom3
Egypt2

+ 13 more countries

Seniority mix

54 of 54 peers have a known seniority level

Senior26
Associate Director26
Principal2

Therapeutic area mix

5 of 54 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology3
Dermatology & Aesthetics2

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
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Senior
Same function Same seniority Same country
60%similar
Amgen Inc. Remote, United States Senior
Same function Same seniority Same country
50%similar
AbbVie Mettawa, IL Associate Director
Same function Adjacent seniority Same country
50%similar
AbbVie Mettawa, IL Associate Director
Same function Adjacent seniority Same country
50%similar
AbbVie Mettawa, IL Associate Director
Same function Adjacent seniority Same country
50%similar
AbbVie Associate Director
Same function Adjacent seniority Same country

Open in 2 locations

Irvine, United StatesNorth Chicago, United States

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%
Senior CMC Regulatory Intelligence Specialist
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Senior
Function Therapeutic area Seniority Country
50%
Associate Director, International Regulatory Affairs Advertising & Promotion
AbbVie · Mettawa, IL · Associate Director
Function Therapeutic area Adjacent seniority Country
50%
Associate Director, Regulatory Affairs US & Canada Strategy Lead – Facial Aesthetics - Device
AbbVie · North Chicago, IL · Associate Director
Function Therapeutic area Adjacent seniority Country
50%
Associate Director, Commercial Regulatory Affairs
E.R. Squibb & Sons,L.L.C. · Princeton, United States · Associate Director
Function Therapeutic area Adjacent 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.