FDA-Regulated Medical Editor & Policy Content Specialist

DRT Strategies, Inc; Silver Spring, Northern (MD, KY); Hybrid; USD 70,000 - 90,000; Full time

Job summary

DRT Strategies, Inc. seeks a Medical Editor to edit and format reviews of marketing applications and policy documents, and to attend FDA stakeholder meetings as needed.

The editor will work with FDA leadership and other offices to ensure accuracy, consistency, and one-voice documentation. The role requires organization, attention to detail, reliability, and the ability to interact with FDA stakeholders across several Offices and Divisions.

Qualifications

• Must obtain and maintain a U.S. government Public Trust clearance.
• Citizenship or lawful permanent residence required.
• No agencies, third parties, or Corp-to-Corp submissions.
• Experience editing medical/marketing applications and FDA policy documents preferred.
• Strong editing and formatting skills with attention to detail.
• Ability to coordinate with FDA stakeholders across offices and divisions.

Responsibilities

• Edit and format reviews of marketing applications and policy documents for consistency.
• Attend and summarize meetings with FDA stakeholders as needed.
• Draft and summarize materials with senior leadership guidance.
• Manage document control with a team of medical editors for one voice.
• Perform literature searches to support editing revisions.
• Conduct routine quality checks on editors' work.
• Organize and update SharePoint sites for project needs.

Skills

Process-oriented

Fast-paced work

Relationship building

Meeting minutes

Organization & time management

Project management

SharePoint

MS Office proficiency

MS Word advanced

Education

Bachelor's Degree

Master's in STEM

Tools

SharePoint

EndNote

Visual Basic

Job description

DRT Strategies, Inc. seeks a Medical Editor to edit and format reviews of marketing applications and policy documents, and to attend FDA stakeholder meetings as needed.

The editor will work with FDA leadership and other offices to ensure accuracy, consistency, and one-voice documentation. The role requires organization, attention to detail, reliability, and the ability to interact with FDA stakeholders across several Offices and Divisions.