About the Role
The Senior Medical Writer will be responsible for developing high-quality clinical and regulatory documents, including clinical study reports, protocols, investigator brochures, and submission documents.
This role involves collaborating with cross-functional teams to ensure accuracy, consistency, and compliance with regulatory standards. The Senior Medical Writer will also provide strategic input into clinical development plans and contribute to publications in peer-reviewed journals.
Salary Range: $114,190 - $141,390.
Requirements
Bachelor's degree in life sciences; advanced degree preferred.
Minimum of 5 years of medical writing experience in the pharmaceutical or biotechnology industry.
Strong understanding of regulatory requirements and guidelines (e.g., ICH, FDA, EMA).
Excellent written and verbal communication skills.
Ability to manage multiple projects and meet deadlines.
Proficiency in Microsoft Office Suite and document management systems.
About Use Our Intel
Use Our Intel is a leading provider of news, analysis, and intelligence for government and industry. With 10 specialized publications, we serve more than 2.2 million unique monthly readers and have a newsletter subscriber base exceeding 1.25 million. In addition to delivering trusted insights in areas like homeland security, global health, and cybersecurity, we offer strategic communications, data analytics, among other services.
Our expertise extends to research and surveys, helping organizations make informed, data-driven decisions. Through our publications, services, and 10 annual branded events, we empower clients with the intelligence they need to navigate complex challenges and drive innovation.