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, and financi…
Skills: Scientific writing, Copy editing, Regulatory history, FDA review process, Medical editing
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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, and financi…
Skills: Medical editing, Scientific writing, Copy editing, Document control, SharePoint
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$100k–$130k/yr
Full-time
postgraduate degree
Posted 3d ago
Apply by Dec 7
~40 hrs/week
Responsibilities
The Scientific Writer will support FDA CBER review staff by preparing post-market memoranda, regulatory history documents, and policy papers. They will also perform copy editing, quality checks, and assist in the development of visual communication aids while ensuring 508 compliance.
Requirements
Candidates must possess a Master’s or PhD degree in biomedical sciences and at least 5 years of scientific writing and copy-editing experience. Familiarity with FDA review processes, style guides, and the ability to obtain a U.S. government Public Trust clearance are required.
Full 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, and financial 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 HR@drtstrategies.com, or by dialing 571-482-2517.
Please be aware of recruitment fraud where malicious individuals might pose as DRT Strategies. Only job postings and emails from drtstrategies.com are authentic and legitimate communications regarding DRT Strategies employment opportunities. Please contact Human Resources at hr@drtstrategies.com if you believe you have received a fraudulent email.
DRT Strategies, Inc. (DRT) is an award-winning technology innovator and leading digital transformation partner to large federal agencies and commercial clients for nearly 20 years. The company is a ServiceNow™ Partner - Specialist, Amazon Web Services (AWS) Consulting Partner, UiPath Partner, SAFe Bronze Partner, Esri Bronze Partner, and holds ISO 9001:2015, ISO/IEC 20000-1:2018, and ISO/IEC 27001:2013 certifications and has achieved CMMI-DEV Level 3.
DRT is headquartered in Arlington, Virginia, with offices in Atlanta, Georgia. More information on the company can be found at www.drtstrategies.com.
Offices: 1001 19th St N, Suite 1200, Arlington, Virginia 22209, US · 5502 Peachtree Rd, Suite 225, Chamblee, Georgia 30341, US
Agile IT ManagementHealth Information ManagementPortfolioProgram & Project ManagementFinancial TransformationStrategy & ChangeTechnology TransformationCybersecurityIT Service Management & ITILServiceNow