Scientific Writer Sr.

• 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.

• 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.

• 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.

• Masters or PhD degree in biomedical sciences

• 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.

• $100000-$130000
• 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 or by dialing .

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