Global Regulatory Lead

TN United Kingdom; Cambridge; Hybrid; GBP 80,000 - 120,000; Full time

Job summary

An innovative global healthcare company is seeking a Global Regulatory Affairs Lead to drive the development and execution of regulatory strategies for their diverse portfolio. This role offers a unique opportunity to influence the regulatory landscape and ensure the successful development of groundbreaking therapies. Join a dynamic team that values creativity and collaboration, while contributing to the advancement of science and improving lives. With a focus on personal and professional growth, this position promises a rewarding career path in a supportive environment.

Benefits

High-quality healthcare

Wellness programs

Parental leave

Career development opportunities

Qualifications

• 12+ years in pharmaceutical/biotech R&D, with 10+ in Regulatory Affairs.
• Expertise in developing innovative regulatory strategies.
• Proven leadership in regulatory filings and registrations.

Responsibilities

• Lead and execute global regulatory strategies for product development.
• Interface with Global Project and Brand Teams for strategic alignment.
• Foster team performance and develop regulatory strategists.

Skills

Regulatory Affairs

Pharmaceutical Experience

Leadership

Strategic Planning

Negotiation Skills

Education

BS/BA in Scientific Discipline

Advanced Degree (PharmD, PhD, MD)

Job description

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• Location: Bridgewater, NJ or Cambridge, MA

About the job:

Our team is involved in developing regulatory product strategies for the Immunology and Inflammation therapeutic area, leading regulatory efforts in the development stage of drug products.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main responsibilities:

1. As Global Regulatory Affairs Lead (GRL), you will be the fully accountable decision maker for the development & execution of creative, thoughtful, and robust global regulatory strategies for your products in Sanofi’s diversified portfolio in order to meet corporate and business objectives.
2. You will be the primary interface and key strategic GRA partner for the Global Project Team (GPT) and Global Brand Team (GBT).
3. Accountable for leading the development and execution of innovative and value-added global regulatory strategies and responsible for formulating the Global Regulatory Project Strategy (GRPS), Global Submission Strategy, and core product labeling in development as well as for lifecycle management of products.
4. Responsible for proactively contributing to the Target Product Profile (TPP), ensuring competitive profiles in alignment with the business objectives.
5. Accountable for leading the GRT for fostering team performance by aligning team on mission, prioritization, objectives and setting clear expectations for the Global Regulatory Strategy and Plan, including a global labeling strategy for assigned projects.
6. Supervise, coach, and facilitate a feedback culture within the GRT to develop team performance.
7. Develop a team of Regulatory Strategists (RS) as appropriate.
8. Accountable for ensuring alignment and communication internally and externally as “one GRA voice” with TA, GBU Head and up to the GRA LT when needed to advocate regulatory position to governance and committees and shares outcomes to GRT and cross-functional partners as appropriate.
9. Identify opportunities to support the team to identify regulatory acceleration opportunities, take thoughtful risks, accept challenges, and make final decisions on the regulatory success rates and mitigations on behalf of the GRT.

About you:

Experience

• At least 12+ years of relevant pharmaceutical/biotechnology experience in R&D, including at least 10 years of relevant Regulatory Affairs experience (regionally and/or global), in early and late development
• Proven record of leading filing/registrations and obtaining regulatory action in major market(s)
• Demonstrated expert regulatory strategic experience and understanding of the regulatory environment to develop regulatory strategies
• Experience being accountable for developing and defending innovative regulatory strategies at Global Project Teams or equivalent forum
• Proven track record of developing innovative regulatory strategies supporting the clinical development of drugs and/or innovative biologics products

Soft Skills

• Lead and leverage talent to the advantage of the greater team, with curiosity and openness to diverse perspectives
• Proactively cultivate a safe environment that inspires creativity, innovation, and productivity
• Proactively accountable for creating a forward-looking vision for your team/direct reports, influence the environment that maximizes long-term potential by fostering trust and teamwork
• Demonstrate exceptional business acumen, strong leadership presence internally and externally, mastery level influence and persuasive negotiation skills
• Master scientific acuity applicable to multiple therapeutic areas
• Proven track record of strategic leadership and significant experience making complex decisions, taking thoughtful risks, and defending difficult positions
• Proven track record and expert (recognized internally and externally) using advanced communication skills (oral and written) to build internal matrix teams and lead complex negotiations with internal and external stakeholders
• Strong sensitivity for a multicultural/multinational environment

Education

• BS/BA degree in a relevant scientific discipline required
• Advanced degree (PharmD, PhD, MD or DVM or MSc in Biology, Life Science, or related field) is preferred.

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military service; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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Pursue, discover

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our and check out our Diversity Equity and Inclusion actions at !