Senior Functional Specialist

• Define project scope, phases, deliverables, milestones, timelines, and measures of success.
• Develop and maintain project plans, trackers, schedules, and support documentation.
• Monitor assignments, action items, dependencies, and deadlines across active projects.
• Identify emerging issues and coordinate follow-up to support timely completion of FDA commitments.
• Compile monthly status updates on project progress, accomplishments, risks, and upcoming activities.

• Conduct literature reviews, environmental scans, and data analyses to support ongoing initiatives.
• Retrieve, review, curate, and organize records from FDA systems and other relevant sources.
• Contribute to the development of Federal Register notices, presentations, speeches, articles, reports, and related communications.
• Draft, revise, format, route, and track documents through internal review and clearance.
• Prepare briefing materials, summaries, and other written products for leadership and project teams.

• Support the development of stakeholder engagement and outreach strategies.
• Coordinate internal and external meetings, including participant outreach, agendas, briefing materials, logistics, and follow-up.
• Document key discussion points, decisions, recommendations, and next steps.
• Support public meetings and workshops through notice development, speaker coordination, registration, logistics, and on-site or virtual assistance.
• Arrange meeting platforms and technology for FDA and stakeholder engagements

• Develop and maintain digital tools, trackers, and workflows for monitoring projects and deliverables.
• Build and manage databases or data repositories needed to support project activities.
• Maintain SharePoint sites, project files, reference materials, and final records.
• Organize and archive meeting summaries, cleared documents, and supporting materials.
• Improve project processes and tools to strengthen coordination, reporting, and information management.

• Respond to staff inquiries and project-related requests in a timely manner.
• Coordinate across project teams to gather updates, resolve information gaps, and support completion of deliverables.
• Provide day-to-day operational support for high-priority and time-sensitive initiatives

• 5+ years of experience supporting the FDA and/or industry

• PMP Certification

• PharmD required

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.

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).

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.

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