Scientific Writer Sr.

DRT Strategies, Inc; Silver Spring, Northern (MD, KY); On-site; USD 100,000 - 130,000; Full time

Job summary

DRT Strategies, Inc. delivers scientific writing and editing support for FDA CBER, with a focus on memo drafting, regulatory history, and manuscript preparation.

The role requires meticulous editing, stakeholder communication, and adherence to FDA review processes. The consultant will produce high-quality documents, manage version control, and coordinate with editors to ensure a single voice across materials.

Qualifications

• 5+ years of scientific writing and copy-editing experience.
• Experience synthesizing and disseminating scientific information regarding complex issues, decisions, or policies.
• Familiarity with a style guide (e.g., AP, Chicago, or AMA).
• Excellent organizational, time management, and communication skills, demonstrated experience working independently as well as in a team environment.
• Ability to take scientific meeting minutes and synthesize discussion points for stakeholders
• Computer skills: MS Office and reference software.
• Intermediate experience and/or certification in Microsoft Word with willingness to learn new features.

Responsibilities

• Work with FDA stakeholders in their review of complex scientific documents including post-market memoranda, manuscripts, policy documents, committee briefings, and slide presentations.
• Draft scientific content including study protocols, white papers, presentations, and manuscripts for submission to peer-reviewed journals.
• Perform copy editing for grammar, punctuation, style, and internal consistency.
• Analyze and evaluate the requirements for assigned writing and editing tasks.
• Perform literature searches as needed to assist with editing and revision of document content.
• Draft, Perform routine quality checks on the work of other medical writers/editors.
• Assist in the development of visual communication aids including graphs, figures, and infographics.
• Work with a team of editors and writers to manage document control, edit and format for consistency and one voice.
• Help customers to identify ineffective or inefficient process areas and to make improvement recommendations.
• Assist DRT to identify other areas where our Health Science practitioners can help current and future customers
• Check document for 508 Compliance.
• Work with FDA stakeholders on requirement gathering, project scope, risks and deliverables.
• Assist with overall project support as needed.

Skills

Scientific writing

Copy-editing

MS Office

Communication

Time management

Meeting minutes

Team collaboration

Education

Master’s or PhD in biomedical sciences

Tools

SharePoint

EndNote

Visual Basic

Microsoft Word

Job description

Overview

DRT Strategies delivers expert management consulting and information technology (IT) solutions to large federal agencies, state and local government and commercial clients in health care, technology, andfinancial services industries.

The three letters of our name, DRT, stand for Driving Resolution Together, which is the core philosophy on which the company was founded. That is, we collaborate with our clients to solve their most pressing challenges - together.

We are problem solvers dedicated to your success, combining Fortune 500 experience with small business responsiveness. We have established a reputation with our clients as a forward-thinking consulting firm with demonstrated success in implementing solutions that lead to meaningful results. Our world-class consultants unite people to work collaboratively to achieve project goals and make vision a reality.

Project Description:

The project provides Scientific writing and medical editing support to the FDA Center for Biologics and Research (CBER). The project supports the FDA’s mission to ensure that safe and effective biologics are available to the American people.

Job Summary:

The Scientific Writer will support FDA CBER review staff prepare post-market memorandum, draft regulatory history, and/or backgrounder documents. Contractor staff will edit and format review memos, manuscripts, and policy documents as well as attend and summarize meetings with FDA stakeholders as needed. The position requires thorough understanding of FDA review process, attention to detail, reliability, consistency, and interaction with FDA stakeholders across several Offices and Divisions.

Responsibilities:

• Work with FDA stakeholders in their review of complex scientific documents including post-market memoranda, manuscripts, policy documents, committee briefings, and slide presentations.
• Draft scientific content including study protocols, white papers, presentations, and manuscripts for submission to peer-reviewed journals.
• Perform copy editing for grammar, punctuation, style, and internal consistency.
• Analyze and evaluate the requirements for assigned writing and editing tasks.
• Perform literature searches as needed to assist with editing and revision of document content.
• Draft, Perform routine quality checks on the work of other medical writers/editors.
• Assist in the development of visual communication aids including graphs, figures, and infographics.
• Work with a team of editors and writers to manage document control, edit and format for consistency and one voice.
• Help customers to identify ineffective or inefficient process areas and to make improvement recommendations.
• Assist DRT to identify other areas where our Health Science practitioners can help current and future customers
• Check document for 508 Compliance.
• Work with FDA stakeholders on requirement gathering, project scope, risks and deliverables.
• Assist with overall project support as needed.

Required Experience:

• 5+ years of scientific writing and copy-editing experience.
• Experience in synthesizing and disseminating scientific information regarding complex issues, decisions, or policies.
• Familiarity with a style guide (e.g., AP, Chicago, or AMA).
• Excellent organizational, time management, and communication skills, demonstrated experience working independently as well as in a team environment.
• Ability to take scientific meeting minutes and synthesize discussion points for stakeholders
• Computer skills: MS Office and reference software.
• Intermediate experience and/or certification in Microsoft Word with willingness to learn new features.

Preferred Experience:

• Prior experience working on vaccines and/or product review process .
• Experience editing guidelines or other policy documents for the federal government.
• Familiarity with SharePoint, EndNote, and Visual Basic.
• Familiarity with 508 compliance.
• Familiarity with FDA regulation of drugs and biological products and EUA and BLA review processes.
• Ability to understand and follow scientific discussion on drugs, side effects, placebo effects, adverse events, and labeling.

Education & Training:

• Master’s or PhD degree in biomedical sciences

Work Authorization, Clearance Requirement, & Additional Information:

• This position requires the ability to obtain and maintain a U.S. government Public Trust clearance. Due to contract requirements, candidates must be U.S. citizens or lawful permanent residents (green card holders) to be eligible.
• No agencies, third parties, or Corp-to-Corp submissions.

Salary Range:

• $100,000-$130,000
• Salary commensurate with experience.

DRT Strategies, Inc. (DRT) follows the guidelines outlined by the Equal Employment Opportunity Commission (EEOC) to provide all employees and qualified applicants employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related conditions, transgender status, and sexual orientation), national origin, age, genetic information, disability, protected veteran status, or any other protected characteristic under federal, state, or local law.

Reasonable accommodations for applicants and employees with disabilities will be provided. If a reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact Human Resources by emailing [e-mail], or by dialing 571-482-2517.

For additional information, please review the Know Your Rights: Workplace Discrimination is Illegal, E-Verify (English), E-Verify (Spanish). Right to Work (English), Right to Work (Spanish).