Project Manager — FDA Adverse Event Records Program

AI Matched Verified Fresh Posting

Project Manager — FDA Adverse Event Records Program

Parsetek, Inc

July 20, 2026

Location: College Park, Maryland, US
Salary: $80,000 - $90,000
Job Type: Full-Time
Seniority Level: Mid-Level

Job Description

Parsetek seeks a Project Manager to lead daily operations of a multi-year FDA program processing adverse event and product complaint reports for FDA-regulated human foods products (foods, dietary supplements, cosmetics). You will manage a team of 8–9 records and drug safety professionals processing ~9,400 reports annually across nine intake formats to a 95% accuracy standard.


Requirements & Responsibilities

  • Responsibilities: Direct daily production operations, queue management, and staff assignments; own all contract deliverables (bi-weekly status reports, monthly performance reports, quarterly QA reports); lead bi-weekly status meetings with the government customer; manage quality control program and corrective actions; ensure continuous telephone/email coverage 8:00 AM–5:00 PM ET; manage transition, onboarding, and personnel actions. Requirements: Bachelor's degree; 5+ years managing federal records management, data operations, or health data programs; experience with recurring federal deliverable schedules and quantitative quality standards; strong client-facing communication. PMP a plus. Washington metro area residency required (periodic on-site in College Park, MD).