Principal Medical Writer – Clinical Focus

🕒 August 13

🌐 United States, Canada – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $142k - $153k / year

⏰ Full Time

🔴 Lead

🏥📝 Medical Writer

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Veristat

WebsiteLinkedInAll Job Openings

501 - 1000 employees

💼 Consulting

🏥 Healthcare

💊 Pharmaceuticals

💰 Private equity on 2021-05

Consulting • Healthcare • Pharmaceuticals

Veristat is a clinical development services company that provides end-to-end, regulatory-focused support for biopharmaceutical and medical device sponsors. The firm offers full-service clinical trial planning and conduct, regulatory affairs and submission support (including NDA/MAA and interactions with agencies like PMDA), statistical and biometrics services, medical writing, pharmacovigilance, and project management for complex therapeutic areas such as oncology, rare diseases, neurology, biologics, and cell & gene therapies. Veristat operates as a B2B partner to biotech and pharmaceutical organizations to reduce development risk and accelerate regulatory approval.

📋 Description

• Independently plan and prepare regulatory documents and medical communications supporting all phases of product development • Organize, analyze, interpret, and present scientific and statistical information according to ICH and other regulatory guidelines • Prepare documents in accordance with company document standards • Work under the direction of Medical Writing management • Collaborate with cross-functional internal and external document production teams

🎯 Requirements

• 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 the minimum experience requirement on a case-by-case basis • Advanced knowledge of ICH and related regulatory guidelines • Excellent written English • Keen attention to detail • Strong interpersonal and communication skills • Experience with Microsoft Office Suite is essential

🏖️ Benefits

• Remote working • Flexible time off • Paid holidays • Medical insurance • Tuition reimbursement • Retirement plans • Applicable bonus • Inclusive culture • Reasonable accommodations and accessible application experience