Posted 2 months ago
Principal Medical Writer
@ Veristat, LLC
Quebec · British Columbia
Overview
Veristat, LLC is hiring a Principal Medical Writer to plan and prepare regulatory documents and medical communications across product development phases. The work involves organizing and presenting scientific and statistical information per ICH and other regulatory guidelines, working with cross-functional teams. The posting states a flexible, largely remote arrangement with paid holidays and benefits that vary by location.
Responsibilities:
- Plan and prepare regulatory documents and medical communications
- Organize, analyze, and interpret scientific and statistical information
- Apply ICH and other regulatory guidelines and company standards
- Collaborate with internal and external document production teams
Requirements summary:
- Bachelor's degree required; science-related field preferred
- Minimum 7 years of medical writing experience in CRO or pharma/biotech
- Advanced knowledge of ICH and related regulatory guidelines
- Excellent written English and keen attention to detail
- Strong interpersonal and communication skills
- Advanced Microsoft Word proficiency
Tools & skills
Benefits mentioned
Source and dates
Employer career site / ATS feed · workday
- Employer posting date
- 2026-09-22
- First seen by our source
- 2026-10-22
- Source record updated
- 2026-10-24
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Senior |
| Department | Physicians & advanced practice |
| Experience | 7+ years |
| Hours per week | 40 (estimated) |
| Work setting | Home, Office |
| Position | Mostly sitting |
| Physical demands | physical low · computer high |
| Languages | English |
| Education | Bachelor’s degree (required) |
| Fields of study | science-related field |
| Perks mentioned | Generous paid time off, Flexible hours, Retirement plan, Tuition support |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Veristat, LLC
Saved company profile
Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.
Full company description
Veristat is the science-first full-service drug and biologic CRO and consultancy that integrates strategic planning, regulatory expertise, and clinical trial execution to rapidly advance the most complex or novel therapies. At Veristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties. Our scientific experts design and conduct the global activities required for any clinical, regulatory, or commercialization program comprehensively and efficiently. With our focus on novel drug development and nearly 30 years of experience, our versatile approach and bold scientific thinking make the impossible possible. Depend on our game-changing expertise and reliable execution for fast results and positive impact to support your biologics and drugs to treat rare cancers, CNS/Neurological disorders, Endocrine/metabolic disorders, and infectious diseases. We are…Bold. Scientific. Versatile. Veristat. - Veristat has recently been made aware that unknown third parties that have no connection to Veristat are generating fake Veristat job postings, interviews, and even fake employment offers via emails, websites, and various social media platforms, seemingly for the purpose of fraudulently obtaining personal information from legitimate job candidates. All legitimate correspondence from Veristat will originate from our applicant tracking system (Jobvite) or an @veristat.com email address. If you have received outreach from someone claiming to be a member of our team please search our official LinkedIn company page (https://www.linkedin.com/company/veristat-llc), where all members of our authorized recruiting team can be identified, or contact us directly at [email protected]. Be vigilant.
- LinkedIn followers
- 32,931
- People associated on LinkedIn
- 494
- Reported office locations
- 134 Turnpike Rd, Ste 200, Southborough, Massachusetts 01772, US
- 2801 Slater Road, Ste 100, Morrisville, North Carolina 27560, US
- TAIPEI, Hsin Ji 9F-1., No.460, Sec. 4 Xinyi Rd., Xinyi Dist., Taipei City, 11052, TW
- 36 rue de l'intendance, Lotissement de l'intendance, Fréjus, 83600, FR
- Carrer de Sant Antoni, Maria Claret 167, Barcelona, 08025, ES
- Aeschenvorstadt 52, Basel, CH-4051, CH
- Business categories
- Life Science
- Medical
- Pharmaceutical
- Other recorded names
- Veristat
- Specialties
- Strategic Consulting
- Safety Management
- Data Management
- Biostatistics
- Statistical Programming
- Project Management
- Medical Writing
- Regulatory Submissions
- Adaptive Clinical Trial Design
- Site Monitoring
- Regulatory Consulting
- Clinical Trial Patient Recruitment
- Clinical Trial Data Standardization
- Clinicl Trial Design
- Clinical Trial Management
- US Regulatory Agent
- Pharmacovigilance
- Marketing Applications Support
- IND Support
- Regulatory Publishing
- Biologic
- Gene Therapy
- Full-service CRO
- and Oncology Clinical Trials
- Profile identifies a recruitment agency
- No
- Reported total investment
- 0
Currency and observation date were not supplied; this is not a current valuation or a funding round.
Veristat is the science-first full-service drug and biologic CRO and consultancy that integrates strategic planning, regulatory expertise, and clinical trial execution to rapidly advance the most complex or novel therapies. At Veristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties. Our scientific experts design and…
| Field | Value |
|---|---|
| Industry | Research Services |
| Company size | 501-1,000 employees |
| Headquarters | Southborough, Massachusetts |
| Organization type | Privately Held |
| Specialties | Strategic ConsultingSafety ManagementData ManagementBiostatisticsStatistical ProgrammingProject ManagementMedical WritingRegulatory SubmissionsAdaptive Clinical Trial DesignSite Monitoring |
| Open jobs on Jobsy | 3 |
| View page |
Job Description:
Principal Medical Writer
The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonisation (ICH) and other regulatory guidelines, and individual company document standards. The Principal Medical Writer works under the direction of Medical Writing management and collaborates with cross-functional internal and external document production teams.
Make an Impact at Veristat!
Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.
· 105+ approved therapies for marketing applications prepared by Veristat
· 480+ oncology projects in the past 5 years
· 350+ rare disease projects delivered in the past 5 years
· Flexible, inclusive culture — 70% remote workforce, 66% women-led teams
· Learn more about our core values here!
What we offer:
· Benefits vary by location and may include:
o Remote working
o Flexible time off
o Paid holidays
o Medical insurance
o Tuition reimbursement
o Retirement plans
What we look for:
• Bachelor’s degree required; science-related field preferred.
• Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case-by-case basis.
• Advanced knowledge of ICH and related regulatory guidelines.
• Excellent written English and keen attention to detail.
• Strong interpersonal and communication skills.
• Experience with Microsoft Office Suite is essential, including advanced Microsoft Word proficiency.
Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.
Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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