Senior Research Analyst, Quality and Compliance (Pharmaceutical, Biotech)

G0549 Politico LLC; Arlington (VA); On-site; USD 90,000 - 130,000; Full time

Job summary

POLITICO is seeking a Senior Research Analyst to help lead parts of AgencyIQ, focusing on drug product quality and FDA compliance. The role is based in Arlington, Virginia, reporting to the Senior Director for Life Sciences Research.

The position requires at least 3 years analyzing FDA regulatory policies with emphasis on quality regulations, a strong writing ability, and experience delivering timely regulatory analyses in fast-paced settings.

Qualifications

• At least 3 years of experience analyzing FDA regulatory policies with emphasis on quality regulations.
• Affinity for writing for business/policy audiences with a passion for regulation.
• Experience delivering daily regulatory analyses in fast-paced, research-driven environments.
• Knowledge of FDA regulatory processes, especially drugs/biotech, and FDA databases.

Responsibilities

• Analyze relevance of regulatory changes and regulatory developments for FDA compliance.
• Produce daily topical intelligence articles for subscribers (3–4 per week).
• Serve as a subject matter expert on drug quality and compliance issues.
• Lead or participate in in-depth analyses, deep-dives, webinars, and newsletters.
• Participate in subscriber and prospect-facing events and briefings.

Skills

Regulatory analysis

Writing

Quantitative analysis

Qualitative analysis

FDA regulatory knowledge

Trend tracking

Fast-paced work

Education

Advanced life sciences degree

Tools

FDA databases

Job description

POLITICO is seeking a Senior Research Analyst to help lead part of its regulatory intelligence and information services product, AgencyIQ, focused on drug product quality and FDA compliance. The role is based in Arlington, Virginia and reports to the Senior Director for Life Sciences Research.

Responsibilities

• Analyze relevance of regulatory changes and developments, track and identify FDA compliance trends, articulate industry impact, and provide context to regulatory professionals.
• Produce daily (3–4 per week) topical intelligence articles and other content for subscribers based on emerging regulatory and legislative developments.
• Serve as a subject matter specialist on drug quality and compliance issues.
• Lead or participate in the development and delivery of in‑depth analysis, deep‑dive research, webinars, and email newsletters.
• Participate in subscriber‑ and prospect‑facing events and briefings.

Required Qualifications

• At least 3 years of experience analyzing FDA regulatory policies at a consulting company, think tank, trade association, government agency, life sciences company, or media outlet with an emphasis on quality regulations.
• Affinity for writing – efficiently and effectively for a business or policy audience – paired with a passion for regulation and regulatory policy.
• Experience and comfort working in fast‑paced, research‑driven environments with daily delivery of written regulatory analyses.
• Experience with qualitative and quantitative analysis and trend tracking.
• Good working knowledge of FDA regulatory processes, especially those related to drugs and biotechnology products, and familiarity with FDA’s compliance systems and databases.
• Capability to deliver expert insights to knowledgeable subscribers.

Preferred Qualifications

• Advanced degree or certification related to the life sciences (PhD, relevant master’s degree, or J.D.).
• Prior experience working in media, including as a journalist or writing a product widely read by others.
• Experience in quantitative analysis using FDA data sets.
• Experience presenting on regulatory topics to a variety of audience types (small groups, large groups) in virtual and in‑person environments.

This role offers the opportunity to work alongside top executives and contribute to a dynamic team. The position requires an organized, motivated, detail‑driven professional who thrives in an in‑office setting.