Remote Principal Medical Writer — Regulatory & Scientific

Veristat; England; Híbrido; GBP 85.000 - 110.000; Tempo integral

Benefícios oferecidos por esta vaga

Remote working

Flexible time off

Medical insurance

Tuition reimbursement

Resumo da vaga

Veristat is seeking a Principal Medical Writer to independently plan and prepare regulatory documents and medical communications for all stages of product development. You will organize and interpret scientific data, ensuring alignment with ICH guidelines and Veristat standards.

In this senior role, you will collaborate with cross-functional teams and reporting lines to support high-quality submissions, while maintaining accuracy, attention to detail and strong written English.

Qualificações

• Bachelor’s degree required; science-related field preferred.
• Minimum of 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.
• Experience with Microsoft Office Suite, including Word proficiency.

Responsabilidades

• Plan and prepare regulatory documents and medical communications for all product development phases.
• Analyze, interpret and present scientific and statistical information per ICH and company standards.
• Collaborate with cross-functional internal and external document production teams.
• Support Medical Writing management and contribute to cross-functional projects.

Conhecimentos

Excellent written English

Interpersonal communication

Communication skills

Formação

Bachelor’s degree in a science-related field

Ferramentas

Microsoft Word

Microsoft Office Suite

Descrição da vaga

Veristat is seeking a Principal Medical Writer to independently plan and prepare regulatory documents and medical communications for all stages of product development. You will organize and interpret scientific data, ensuring alignment with ICH guidelines and Veristat standards.

In this senior role, you will collaborate with cross-functional teams and reporting lines to support high-quality submissions, while maintaining accuracy, attention to detail and strong written English.