Associate Director, Research – European Pharmaceuticals and Biotechnology Regula
POLITICO, Arlington, VA, United States
Associate Director, Research – European Pharmaceuticals and Biotechnology Regulation
POLITICO is seeking an
Associate Director, Research
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. Our written research and analysis is relied upon by many top companies, trade groups, law firms, and advocacy groups to help them understand breaking news, identify emerging trends, predict future action, and prepare for seismic shifts in regulatory policy.
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 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)
#J-18808-Ljbffr
Associate Director, Research
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. Our written research and analysis is relied upon by many top companies, trade groups, law firms, and advocacy groups to help them understand breaking news, identify emerging trends, predict future action, and prepare for seismic shifts in regulatory policy.
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 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)
#J-18808-Ljbffr