Associate Director, Research – European Pharmaceuticals and Biotechnology Regulation

G0549 Politico LLC; Arlington (VA); Hybrid; USD 110,000 - 140,000; Full time

Job summary

G0549 Politico LLC in Arlington, VA is hiring an Associate Director, Research to provide insights on European pharmaceuticals and biotechnology regulation. The ideal candidate will have at least 7 years of experience and advanced knowledge in European regulatory processes.

This role involves producing daily articles, deep-dive research, and collaboration with the research team. Additional qualifications include excellent writing skills and the ability to work in fast-paced environments.

Qualifications

• At least 7 years of experience in the field.
• Advanced knowledge of European regulatory processes.
• Experience in fast-paced, research-driven environments.

Responsibilities

• Produce daily topical intelligence articles on regulations.
• Serve as a subject matter specialist in the relevant field.
• Collaborate with the research team for written content delivery.

Skills

Analyzing European life sciences regulatory policies

Excellent writing skills

Qualitative and quantitative analysis

Trend tracking

Education

PhD or master’s degree related to life sciences

Job description

Associate Director, Research – European Pharmaceuticals and Biotechnology Regulation

POLITICO seeks an experienced regulatory expert to support its AgencyIQ product focused on European life sciences regulation.

Responsibilities

• Produce 3–4 daily topical intelligence articles on emerging regulatory developments.
• Serve as a subject matter specialist on European pharmaceutical, biopharmaceutical, biotechnology, biosimilars, generic, and non‑prescription products.
• Lead or participate in in‑depth analysis, deep‑dive research, webinars and email newsletters.
• Participate in subscriber‑ and prospect‑facing events and briefings.
• Collaborate with the research team to deliver written content daily, weekly insights, directed deliverables, and presentations.

Qualifications

• At least 7 years of experience analyzing European life sciences regulatory policies at a consulting firm, think tank, trade association, government agency, life sciences company, or media outlet.
• Advanced‑level knowledge of European regulatory processes for drugs and biotechnology products, and the ability to deliver expert insights to a knowledgeable audience.
• Excellent writing skills for a business or policy audience, clear and concise communication.
• Experience with qualitative and quantitative analysis and trend tracking.
• Comfortable working in fast‑paced, research‑driven environments with daily written delivery.
• Additional: advanced degree or certification related to life sciences (e.g., PhD, master’s degree, or J.D.); media/journalism experience; quantitative analysis using EMA datasets; experience presenting to diverse audiences.

Location

The role can be based at POLITICO headquarters in Arlington, VA, or at the European offices in London or Brussels.

Equal Opportunity Employment. POLITICO is an equal‑opportunity employer.