Senior Medical Writer - Regulatory Submissions & Cross-Functional Lead

kozmetickesluzby.vecnakraska.sk - Jobboard; Lexington (MA); On-site; USD 85,000 - 110,000; Full time

Job summary

Novo Nordisk seeks a Senior Medical Writer in Lexington, Massachusetts. This role involves managing written deliverables essential for clinical development and regulatory requirements.

Qualified candidates will have a minimum of 7 years of relevant experience, with strong skills in communication and project management. Join a global team that values collaboration and attention to detail in clinical documentation.

Qualifications

• Minimum of 7 years relevant experience, with at least 5 years in clinical/regulatory writing.
• Strong foundation in scientific knowledge relevant to medical writing.
• Experience in the pharmaceutical or biotechnology industry preferred.

Responsibilities

• Manage preparation of written deliverables for clinical development.
• Author and edit documents for clinical trials and regulatory submissions.
• Lead discussions and ensure decisions on medical writing issues.

Skills

Exceptional written and oral communication skills

Understanding of clinical research principles

Attention to detail

Scientific knowledge

Adaptability across time zones

Project management skills

Education

BS/BA in health-related or scientific discipline

Job description

Novo Nordisk seeks a Senior Medical Writer in Lexington, Massachusetts. This role involves managing written deliverables essential for clinical development and regulatory requirements.

Qualified candidates will have a minimum of 7 years of relevant experience, with strong skills in communication and project management. Join a global team that values collaboration and attention to detail in clinical documentation.