Medical Writer

This is a fully remote position, open to applicants in United States.

📋 Description

• Executes all tasks associated with the creation of specified medical and regulatory documentation.

• Assists in preparing documents for regulatory submissions to both US and international health authorities.

• Works collaboratively with cross-functional team members to ensure the precise and timely preparation and delivery of high-quality documents.

• Aids in maintaining transparency and disclosures for clinical trials.

• Enhances departmental growth by providing editorial and review assistance for document templates.

⛳️ Requirements

• Bachelor’s degree is required in a scientific field.

• At least 3 years of experience in medical writing within a Sponsor or CRO environment.

• AMWA certification is preferred.

• Proficient in using medical writing systems and tools, including Veeva RIM.

• Familiarity with drug development processes, study conduct protocols, ICH guidelines, and FDA/EU regulations, or proven success in a regulated industry setting.

🏝️ Benefits

• Options for remote work.

• Opportunities for professional development.

• A diverse and inclusive workplace culture.