Jobs / Japan / Regeneron Pharmaceuticals INC

Regeneron Pharmaceuticals INC

Principal Medical Writer, Medical Writing

Tokyo Posted today

Apply on employer site ↗ Tailor my CV first Source: Company careers site

Optional: we can tailor a CV and cover letter for this job from your real experience first (the first one is free).

Skills this job asks for

StatisticsCommunicationRecruitment

Add your CV (free) to see which of these your CV is missing.

Sponsorship verdict

No sponsorship evidence yet

No government record and no wording either way. Not a refusal: ask the recruiter.

  • No government sponsor record hereNo government sponsor record covers this employer in this country.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • Can’t check pay against the visa rulesWe don’t have visa salary rules for this country yet.
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources

A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.

Before you apply

Sponsorship unknown

No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.

These come from the posting’s own wording. Read the original listing to confirm. See better-fit alternatives →

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 Principal Medical Writer to join our Medical Writing team, supporting Global Development in a hybrid work model. In this role, you will lead clinical document strategy and development for assigned compounds while collaborating with Medical Directors, Biostatisticians, Regulatory Liaisons, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & where: Location: Tarrytown, Warren, Uxbridge, Dublin, Tokyo, or Remote Work model: Hybrid Discover your role: • Lead clinical document strategy for assigned compounds across therapeutic areas. • Drive development of CSRs, protocols, ICFs, Investigator’s Brochures, narratives, and regulatory documents. • Lead submission document writing with Medical Directors, Biostatisticians, and Regulatory Liaisons. • Represent Medical Writing in document development meetings and guide strategy discussions. • Oversee junior and outsourced medical writers while contributing independent authoring. • Review Statistical Analysis Plans and TFLs for clinical document content. • Contribute to Medical Writing and Global Development process improvement initiatives. • You build collaboration, resolve challenges, and keep complex projects moving forward. This role requires: • Bachelor’s degree required; advanced degree preferred. • Minimum 7 years of medical writing experience, including strong biostatistics knowledge. • Expert knowledge of clinical research processes, regulations, and guidelines. • Expert experience reading, writing, and editing clinical documents. • Experience authoring regulatory submission documents, including Module 2 documents. • Thorough understanding of ICH Good Clinical Practice guidelines. • Knowledge of applicable guidelines, templates, and SOPs for medical writing. • Proficiency with Microsoft Word, Adobe Acrobat, PowerPoint, and electronic document management systems. • Ability to manage multiple projects and competing priorities. • Excellent organizational, interpersonal, and communication skills. • Management experience preferred. 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, equ

Apply on employer site ↗