Job Description:As a subject matter expert in
the regulation of pharmaceuticals, biopharmaceuticals and biotech in Europe - by the European Medicines Agency and other European regulatory authorities - the Associate Director will be responsible for analyzing the relevance of regulatory changes and developments, articulating the type and degree of impact on industry, and providing context to an audience of knowledgeable regulatory professionals.
We're looking for a regulatory expert who is as knowledgeable about regulatory topics as they are capable of explaining complex subjects to others quickly and effectively.
Reporting to the Senior Director for Life Sciences Research, the Associate Director will join a team of experienced researchers responsible for producing a mix of daily written content, in-depth written research, weekly insights, directed deliverables and presentations.
This role can be based at POLITICO's headquarters in Arlington, Virginia or at POLITICO's European offices in London or Brussels.
What You'll Do - Produce daily (3-4 per week) topical intelligence articles and other content for our subscribers based on emerging regulatory and legislative developments and trends
- Serve as a subject matter specialist on matters of related to how European life sciences regulatory agencies regulate pharmaceuticals, biopharmaceuticals, biotechnology products, biosimilars, generic drugs, and nonprescription products
- 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 regular briefings
What you'll need - At least 7 years' experience analyzing European life sciences regulatory policies at a consulting company, think tank, trade association, government agency, life sciences company, 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 of European regulatory processes related 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 of written regulatory analyses of new information is the norm
- Experience with qualitative and quantitative analysis and trend tracking
While not required, you will stand out if you: - Have an advanced degree or certification related to the life sciences (i.e., a PhD, relevant master's degree, or J.D.)
- Have prior experience working in media, including as a journalist or writing a product widely read by others (i.e., a business intelligence product or internal newsletter)
- Have experience in quantitative analysis using EMA data sets
- Experience presenting on regulatory topics to a variety of different audience types (small groups, large groups) in different environments (virtual and in-person)
