Job Description

Public Trust: NACI (T1)

Requisition Type: Regular

Your Impact

Own your opportunity to work alongside federal civilian agencies. Make an impact by providing services that help the government ensure the well being of U.S. citizens.

Job Description

GDIT's Military Health team is hiring a Medical Writer to support the Office of Regulated Activities (ORA) under the DoD (Dept. of Army) located at Ft. Detrick in Frederick, Maryland. The Office of Regulated Activities (ORA) is a multidisciplinary team of regulatory affairs, compliance, and clinical support professionals dedicated to supporting the USAMRDC mission of developing Food and Drug Administration regulated medical products for the Warfighter. The ORA provides full-service, oversight, and consultation for regulatory, clinical, non-clinical, manufacturing, data management, biostatistics, product technical, safety monitoring.

HOW YOU WILL MAKE AN IMPACT:

• Write, review, edit, and advise on the development of documents and dossiers in an electronic Common Technical Document (eCTD) format, to include IND applications, master files, investigational new device applications, biologics license applications, new drug applications, annual reports, information amendments, clinical protocols and study reports, investigator’s/investigational brochures, FDA meeting requests and background materials, responses to FDA requests for information, target product profiles, clinical development plans, manuscripts, white papers, 510k pre-market notifications, and to a lesser extent pre market approvals, and Environmental Protection Agency registration packages.
• Use eCTD format, MS Word, and applicable templates and standards to produce documents and dossiers compliant with FDA and Office of Regulated Activities (ORA) regulations and standards.
• Lead and manage writing projects.
• Track and meet deadlines for writing projects.
• Attend, participate in, and organize meetings.
• Provide routine reports and updates to team members, project managers, and Government leaders.
• Provide subject matter expertise on regulatory documentation and version control.
• Participate in special projects as required.

WHAT YOU’LL NEED TO SUCCEED:

• Bachelor’s Degree in Science field or a related discipline, or the equivalent combination of education, professional training, or work experience.
• 5 years of related medical or regulatory writing experience.
• Experience writing investigational new drug (IND) application documents in Common Technical Document (CTD) format
• Proven editorial and MS Word formatting skills
• Project management skills, including the ability to be proactive, multi-task, work collaboratively in a team environment, and meet deadlines.
• Knowledge of current regulatory guidelines related to regulatory communications
• The ability to work independently and as part of a team and oversee the activities related to US Food and Drug Administration (FDA) dossier preparation
• Have excellent Microsoft Office skills and experience with eCTD formatting.
• Excellent written and oral communication skills.
• Must be a US Citizen with the ability to obtain a favorable NACLC T3 security investigation prior to start date.
• This is a hybrid position and will report onsite 1-2 days a week at Ft. Detrick in Frederick, Maryland. Must reside within commuting distance.

WHAT GDIT CAN OFFER YOU:

• Challenging work that makes a real impact on the world around you  
• Internal mobility team dedicated to helping you own your career 
• 401K with company match 
• Diverse, highly collaborative teams
• Professional development, education assistance, certification and training opportunities

Work Requirements

Years of Experience

5 + years of related experience

* may vary based on technical training, certification(s), or degree

Certification

Travel Required

None

Citizenship

U.S. Citizenship Required

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