Associate Director, Regulatory Science, EEMEA

Moderna; City Of London; Hybrid; GBP 90,000 - 120,000; Full time

Job summary

A leading biotechnology company in London is seeking an Associate Director, Regulatory Affairs to define strategic regulatory operations across the EEMEA region. The ideal candidate will navigate complex regulatory challenges, drive policy strategies, and collaborate across functions. The role requires over 10 years of experience in regulatory affairs, expertise in biologics, and strong communication skills. This position offers competitive benefits and a hybrid work model.

Benefits

Quality healthcare and insurance benefits

Lifestyle Spending Accounts

Free premium wellness classes

Generous paid time off

Savings and investment options

Location-specific perks

Qualifications

• 10+ years of experience in Regulatory Affairs or related field.
• Expertise in biologics, vaccines, and oncology.
• Fluency in English; knowledge of Arabic is a plus.
• Experience with major regulatory submissions.

Responsibilities

• Define and contribute to the strategic direction of Regulatory Affairs.
• Shape regulatory policy and engagement strategy.
• Engage with regulatory authorities to influence decisions.

Skills

Regulatory Affairs expertise

Communication skills

Analytical skills

Knowledge of EEMEA regulations

Leadership ability

Education

Degree in Life Science or related discipline

Advanced degree preferred (PharmD, MSc, PhD)

Job description

Overview

Joining Moderna offers the opportunity to be part of a pioneering team revolutionizing medicine through mRNA technology, with a diverse pipeline across diseases. You will be part of a growing organization, working with exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna is expanding its presence in London; the office focuses on commercial operations to deliver products to the UK market.

As Associate Director, Regulatory Affairs for the EEMEA region, you will steer the strategic direction of regulatory operations across Eastern Europe, the Middle East, and Africa. You will influence policy and practice, working cross-functionally to ensure regulatory strategy aligns with Moderna’s long-term goals for mRNA therapeutics. This role is an individual contributor position requiring creativity, leadership, and precision in a fast-moving regulatory landscape.

Responsibilities

Key responsibilities

• Define and contribute to the strategic direction of Regulatory Affairs across the EEMEA region.
• Shape regulatory policy and engagement strategy, aligning with Moderna’s long-term objectives.
• Partner with internal and external stakeholders to integrate regulatory strategy with regional and global business goals.
• Exercise regulatory leadership and decision-making authority in a highly matrixed environment.
• Act as a thought partner to the EEMEA Regulatory Affairs Director and support oversight of submissions and agency interactions.

Your responsibilities will also include

• Identify, assess, and solve complex regulatory challenges across functions and geographies using advanced analytical and strategic skills.
• Drive cross-functional initiatives and promote seamless collaboration across teams to accelerate regulatory success.
• Proactively engage with EEMEA regulatory authorities and local partners to influence business-critical decisions and policy development.
• Help manage regulatory impacts on sub-functions and cross-regional processes beyond direct project involvement.
• Maintain awareness of the evolving regulatory landscape and integrate emerging requirements into Moderna’s EEMEA regulatory framework.

Key Moderna Mindsets

• We obsess over learning. We don’t have to be the smartest—we have to learn the fastest. Navigating varied and evolving regulatory environments in EEMEA demands continuous learning, flexibility, and the ability to synthesize new data rapidly. Success relies on embracing complexity and turning it into opportunity.
• We behave like owners. The solutions we’re building go beyond any job description. This role requires a sense of ownership that extends beyond regulatory operations. You will be empowered to shape long-term strategies, guide decision-making, and drive impact across Moderna’s global platform.

What you’ll bring to the table

• Degree in Life Science or related discipline (e.g., Pharmacy, Biology, Biochemical, Bioengineering); advanced degree preferred (PharmD, MSc, PhD).
• 10+ years of experience in Regulatory Affairs or related field.
• Expertise in biologics, vaccines, Rare or Autoimmune Diseases, and Oncology, with strong knowledge of current EEMEA regulations.
• Proven ability to navigate the regulatory landscape, including knowledge of EEMEA, US, and EU regulations for biologic products.
• Exceptional communication skills, with fluency in English; Arabic language is a distinct advantage.
• Dynamic, collaborative approach to working in a cross-functional matrix environment with a bold, curious, and collaborative mindset.
• Experience with preparation of major regulatory submissions and supportive amendments or supplements.
• Ability to collaborate effectively in a dynamic, cross-functional matrix environment to meet program regulatory milestones.

Benefits

• Quality healthcare and insurance benefits
• Lifestyle Spending Accounts to support well-being
• Free premium access to fitness, nutrition, and mindfulness classes
• Family planning and adoption benefits
• Generous paid time off, including vacation, holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
• Savings and investments options
• Location-specific perks and extras

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna

Since 2010, Moderna has aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We are committed to creating a culture of belonging and building an organization that cares deeply for patients, employees, the environment, and communities.

We have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

Moderna champions an in-person culture with a 70/30 in-office work model to foster innovation, teamwork, and mentorship. Join us to learn, contribute, and make an impact.

For current opportunities, please visit the Moderna careers page: modernatx.com/careers

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Moderna is committed to equal opportunity in employment and non-discrimination for all applicants without regard to race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other protected characteristic. Qualified applicants are considered regardless of criminal histories, consistent with legal requirements.

Moderna is committed to offering reasonable accommodations or adjustments to qualified job applicants with disabilities. For accommodations, contact the Accommodations and Adjustments team at [e-mail].