Remote Senior Medical Writer, Regulatory Documents

Veristat; United States; Remote; USD 142,000 - 153,000; Full time

Benefits offered by this job

Remote working

Flexible time off

Paid holidays

Medical insurance

Tuition reimbursement

Retirement plans

Job summary

Veristat seeks a Principal Medical Writer to independently plan and prepare regulatory documents across all product development stages, applying ICH guidelines and Veristat standards. You will organize, analyze, and present complex scientific data in clear, publication-ready formats, collaborating with cross-functional teams under Medical Writing management to deliver high-quality documents.

This role offers a collaborative, flexible environment with a global team experienced in diverse

Qualifications

• Bachelor’s degree in a science-related field (required).
• Minimum of 7 years of medical writing experience in CRO or pharma/biotech settings.
• Advanced knowledge of ICH and related regulatory guidelines.
• Excellent written English and strong attention to detail.
• Strong interpersonal and communication skills.
• Experience with Microsoft Office Suite is essential, including advanced features.

Responsibilities

• Plan and prepare regulatory documents and medical communications for all product development stages.
• Organize, analyze, interpret, and present scientific and statistical information per ICH guidelines.
• Collaborate with cross-functional internal and external document production teams under Medical Writing management.

Skills

Regulatory writing

ICH guidelines

Attention to detail

Written English

Interpersonal communication

Microsoft Office

Education

Bachelor’s degree in science-related field

Tools

Microsoft Office Suite

Job description

Veristat seeks a Principal Medical Writer to independently plan and prepare regulatory documents across all product development stages, applying ICH guidelines and Veristat standards. You will organize, analyze, and present complex scientific data in clear, publication-ready formats, collaborating with cross-functional teams under Medical Writing management to deliver high-quality documents.

This role offers a collaborative, flexible environment with a global team experienced in diverse