Director, Head of Global Nemluvio Regulatory Strategy

About the Company

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ—the skin—meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. We look for people who focus on getting results, embrace learning, and bring positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day.

We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

About the Role

Leads the global regulatory strategy, submission planning, and health authority engagement for Nemolizumab across all approved and development-stage indications, ensuring regulatory activities are executed in accordance with global regulatory requirements, corporate objectives, and agreed timelines. Accountable for the Global Regulatory Affairs team supporting nemolizumab and for driving successful regulatory outcomes across the product lifecycle.

Responsibilities

• Accountable for global regulatory strategies and global submission plans for Atopic Dermatitis (AD), Prurigo Nodularis (PN), and any newly identified indications.
• Leads Nemluvio Global Regulatory Team, establishing team goals, norms, responsibilities, and communication plans.
• Accountable for US regulatory strategies for all indications in coordination with the US Regulatory Affairs Team.
• Primary contact for FDA.
• Identify and assess risks associated with product development and recommend strategies to mitigate these risks.
• Core member of Nemluvio Global Project Team, providing regular updates to leadership, Nemolizumab product strategy team, and commercial teams.
• Ensure strategic regulatory input is provided to key development activities and documents, including clinical, non-clinical, and CMC development documentation as needed.

Requirements

• Knowledge and understanding of regulatory requirements for pharmaceutical/biological product development and approval in more than one key region (e.g., US and EU).
• 10 years of experience communicating the regulatory strategy, issues, and risks in written and verbal format to regulatory senior leadership teams and other governing bodies.
• Experience interfacing with regulatory agencies and skill at implementing successful global regulatory strategies.
• Experience documenting regulatory strategies in coordination with clinical plans and marketing objectives.
• Excellent team interaction skills along with demonstrated ability to work on a cross-functional team.
• Experience with international project management.
• Focused on effective delivery of objectives, even when working with tight deadlines.
• Ability to identify opportunities/major issues and communicate impact.
• Demonstrated ability to deal with rapid change.

Physical Requirements and Work Environment

This role requires the ability to perform standard office activities, including extended periods of computer use, participation in virtual and in-person meetings, and collaboration across teams. Depending on business needs, occasional travel may be required. Work environments and physical requirements may vary based on the requirements of the role. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role.

Pay

The target base salary range for this role is $200,000–$265,000 per year. This range reflects the anticipated compensation for the role. Where pay falls within the range may vary based on many factors, including, but not limited to, job responsibilities, skills, experience, education, certifications, location, and applicable geographic pay zones, market conditions, internal equity, and business considerations. Compensation decisions are made based on an assessment of the candidate’s qualifications and the totality of relevant factors. In addition to base salary, this role is eligible to participate in an annual short-term and long-term incentive program, subject to plan terms and eligibility requirements.

Benefits

Galderma offers a competitive and comprehensive benefits program, including:

• Medical, dental, and vision coverage.
• A 401(k) plan with employer match.
• Paid time off.
• Other benefits, subject to eligibility and applicable plan terms.

Work Authorization

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.