POLITICO is seeking a Senior Research Analyst to help lead part of its regulatory intelligence and information services product, AgencyIQ. Since its founding in early 2020, AgencyIQ has quickly become the premier source of regulatory intelligence and analysis for professionals working in the life sciences, foods and chemicals industries and is relied upon by many top companies, trade groups, law firms and advocacy groups.
As a subject matter specialist in the regulation of pharmaceuticals, biopharmaceuticals and biotech by the U.S. Food and Drug Administration (FDA), the Senior Research Analyst 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.
The Senior Research Analyst 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 position would be partially remote, with an expectation of in-office work 12 days per month at POLITICO’s headquarters in Arlington, Virginia.
Who You Are:
- A subject matter expert with deep knowledge of FDA regulatory frameworks, particularly in pharmaceuticals, biopharmaceuticals, and biotechnology
- A sharp analytical thinker who can assess regulatory developments and communicate nuanced impacts clearly and confidently to a sophisticated professional audience
- An exceptional communicator with strong writing skills and the ability to produce high-quality daily content, in-depth research, and strategic insights
- A collaborative team player who thrives in a fast-paced, research-driven environment and values cross-functional engagement across scientific domains
- Comfortable engaging with external stakeholders through webinars, presentations, and industry briefings
- Curious and forward-looking, with a passion for staying ahead of regulatory trends and translating complexity into actionable intelligence
What You’ll Do:
- Produce daily topical intelligence articles and other content for our subscribers based on emerging regulatory and legislative developments related to the FDA’s regulation of pharmaceuticals, biopharmaceuticals and biotechnology products
- Serve as a subject matter specialist on several regulatory topics for AgencyIQ (e.g., gene therapy, novel drug approvals, post-marketing assessments, etc.)
- Lead or participate in the development and delivery of in-depth analysis, deep-dive research, webinars and email newsletters
- Collaborate with other members of AgencyIQ’s research team focused on chemical, food and life sciences regulation
- Participate in subscriber- and prospect-facing events, briefings, and business development activities
What You’ll Need:
- At least 4 years’ experience analyzing FDA regulatory policies at a consulting company, think tank, trade association, government agency, or life sciences company
- 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.
- Experience and comfort working in fast-paced, research-driven environments in which daily delivery of written regulatory analyses is the norm
- A good working knowledge of FDA regulatory processes (and in particular those related to drugs and biotechnology products); capable of delivering expert insights to our knowledgeable subscribers
- Experience presenting on regulatory topics to a variety of different audience types (small groups, large groups) in different environments (virtual and in-person)
- Advanced degree or certification related to the life sciences, law or policy (i.e., a JD, PhD, relevant master’s degree and/or your RAC) preferred.
- 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) preferred.
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