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Associate Director, Research – European Pharmaceuticals and Biotechnology Regulation

ArlingtonOn-siteFull-time

AI Summary

Analyzes European pharmaceutical and biotechnology regulation for POLITICO's AgencyIQ product, producing daily intelligence articles and in-depth research for life sciences professionals.

About this role

Job Description:

POLITICO is seeking anAssociateDirector,Researchto help lead part of its regulatory intelligence and information services product,AgencyIQ.Since its founding in early 2020,AgencyIQhas quickly become the premier source of regulatory intelligence and analysis for professionals working in the life sciences,foodsand chemicals industries.

Our written research and analysisisrelied upon by many top companies, trade groups, law firms and advocacy groupsto help them understand breaking news,identifyemerging trends, predict futureactionand prepare for seismic shifts in regulatory policy.

As a subject matterexpertinthe regulation ofpharmaceuticals, biopharmaceuticals and biotechin Europe–bythe European Medicines Agency and other European regulatory authorities–theAssociate Directorwill be responsible for analyzing the relevance of regulatory changes and developments, articulating the type and degree of impact onindustry, and providing context to an audience of knowledgeable regulatory professionals.

We’re lookingfor a regulatory expert whois asknowledgeable about regulatory topics as they are capable of explaining complex subjects to othersquickly and effectively.

Reporting to the Senior Director for Life Sciences Research, theAssociate Directorwill join a team of experienced researchers responsibleforproducing a mix of dailywrittencontent, in-depthwrittenresearch, weekly insights, directed deliverables and presentations.

This role can be based at POLITICO’s headquarters in Arlington, Virginiaor at POLITICO’s European offices in LondonorBrussels.

WhatYou’llDo

  • Produce daily(3-4 per week)topical intelligence articles and other content for our subscribers based on emerging regulatory and legislative developmentsand trends

  • Serve as a subject matter specialist onmatters ofrelated to how European life sciencesregulatory agencies regulate pharmaceuticals, biopharmaceuticals, biotechnology products, biosimilars, generic drugs, and nonprescription products

  • Lead orparticipatein the development and delivery of in-depth analysis, deep-dive research,webinarsand email newsletters

  • Participate in subscriber- and prospect-facing eventsandregularbriefings

Whatyou’llneed

  • At least7years’ experience analyzingEuropean life sciencesregulatory policiesat a consulting company, think tank, trade association, government agency,life sciencescompany, or media outlet

  • An affinity for writing – efficiently and effectively, and for a business or policy audience – paired with a knowledge of (and passion for) regulation and regulatory policy

  • Advanced-level (and preferably expert-level)knowledge ofEuropeanregulatory processesrelated to drug and biotechnology products; capable of delivering expert insights to our knowledgeable subscribers

  • Experience and comfort working in fast-paced, research-driven environments in which daily delivery ofwrittenregulatory analysesofnew informationis the norm

  • Experience with qualitative and quantitative analysis and trend tracking

While notrequired,you will stand outif you:

  • Have an advanced degree or certification related tothelifesciences(i.e., a PhD, relevant master’s degree, or J.D.)

  • Have prior experience working in media, including as ajournalistor writing a product widely read by others (i.e., a business intelligence product or internal newsletter)

  • Haveexperience in quantitative analysis usingEMAdata sets

  • Experience presenting on regulatory topics to a variety of different audience types (small groups, large groups) in different environments (virtual and in-person)

We value our people. Click here for more on what we offer and what it’s like to work for POLITICO.
Let’s keep in touch. You can view our list of open positions here.

About Us.

POLITICO illuminates the forces shaping global power. Since 2007, we have delivered intelligence that anticipates tomorrow's headlines, not reports on yesterday's news. As politics has increasingly become the defining force of our era, our work has never been more vital.

Cabinet secretaries and Ministers start their mornings with our analysis. CEOs shape strategy around our reporting. Advocacy leaders rely on our insights to move policy. We deliver the straightforward facts and clear-eyed analysis they need to navigate the most complex political landscape of our lifetimes.

Our 1,100+ publishing professionals across the world's key democratic capitals—Washington, Brussels, London, Paris, Berlin, Sacramento, and New York—form the world's premier politics and policy newsroom. We tell the story of how power really works by explaining who wields it and how they plan to exercise it, connecting dots others miss and delivering scoops from sources others don't even know exist.

Innovation has always been a core tenet of our story. At launch, we bet that depth would trump scale, that talent would trump traffic, and that politics would become central to modern life. In 2011, we made another bet and launched POLITICO Pro to help decision-makers understand the business of government, transforming both how they shape government action and the business of journalism itself.

These bets have made POLITICO the most successful digital news startup of its generation and the indispensable resource for leaders who shape the future. Today, we are a rarity in media: a growing, profitable, and sustainable news organization.

POLITICO is a subsidiary of Axel Springer SE, a family-owned transatlantic media company headquartered in Berlin and New York. Axel Springer is dedicated to shaping the future of journalism in the free world, believing that a free and informed society is essential to democracy. The company’s guiding principles - first articulated as The Essentials by founder Axel Springer in the aftermath of World War II - remain a cornerstone of the company’s foundation today. Learn more about Axel Springer.

Posting date:

2026-04-07

Title:

Associate Director, Research – European Pharmaceuticals and Biotechnology Regulation

Skills

BiosimilarsBiotechnology RegulationEMA Data SetsEuropean Medicines Agency (EMA)European Regulatory ProcessesGeneric DrugsLife Sciences Regulatory PolicyPharmaceutical RegulationQualitative AnalysisQuantitative AnalysisRegulatory IntelligenceTrend Tracking

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