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. #J-18808-Ljbffr