US Regulatory Strategy lead

At Sobi, we believe diversity drives innovation and inclusion creates stronger teams. We are committed to building a workplace where everyone feels valued and empowered to contribute. If this role excites you but you’re unsure if you meet every requirement, we encourage you to apply. Your unique perspective and experiences could be exactly what we need.

At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients.

About the Role

The US Regulatory Strategy Lead is responsible for all aspects of the US Regulatory Strategy for assigned development and marketed products. This role is a critical member of the Global Regulatory Team (GRT), providing US-focused product strategy, US regulatory framework knowledge, and awareness of external regulatory initiatives. The US Regulatory Strategy Lead partners with the Global Regulatory Lead (GRL) and participates on cross-functional project teams, including MDT and CAT, representing Regulatory on an agenda-driven basis. The role involves presenting the US regulatory position on assigned products to Sobi stakeholders and developing US regulatory strategies, including risk assessments, mitigation strategies, and championing expedited regulatory pathways for accelerated patient access in the US.

Responsibilities

• Core member of the GRT, collaboratively working with the team to weave US strategies into global strategies as they are developed.
• US participant on Sobi Product Cross Functional Teams as appropriate.
• Point of contact within GRA on the core asset team (CAT) and Medicines Development Team (MDT) for assigned program(s).
• Ensures guidance on regulatory pathways to accelerate product development (e.g., ODD, FTD, Accelerated Approval, Priority Review, etc.) is evaluated and included where possible in the US Strategy.
• Prepares cross-functional team for any major FDA Meetings and leads/facilitates major meetings with the Agency.
• Leads triage process for any FDA Information Requests or Health Authority Communications that require Sponsor Response to FDA.
• Contributes to Submission Taskforce meeting and efforts to ensure timely and quality submissions of major application(s) is executed successfully.
• Point of contact and lead with regulatory consultants and facilitates meetings and any communications shared between regulatory and its consultants.
• Cooperates with other departments and affiliates within Sobi, regulatory authorities, partners, and regulatory consultants.
• Key contact for FDA on product(s) and with direct FDA interaction. Ensures communications from FDA are properly communicated to the business after assessing the feedback and outlining next steps.
• Key contact for development and business partners on product(s).
• Contributes to US product labeling, working with the GRL and Labeling group to ensure core label changes are appropriately conveyed in US product labeling; Partners with US Commercial and Ad Promo Team.
• Responsible for IND, NDA, and BLA submissions to FDA in partnership with Regulatory Operations.
• Regulatory representative on due diligence assessments of new business opportunities as required.
• Reviews regulatory SOPs as needed.
• Participates in operational excellence work (improvement projects) as needed.
• May represent Sobi on industry work events and attend public meetings.
• Monitors and assesses impact of relevant US regulations, guidance, and current regulatory environment.

Requirements

• BS in a scientific discipline. Advanced degree (PhD, PharmD, MD) preferred but not required.
• 6+ years regulatory affairs experience having led health authority meetings (FDA). Ideal candidate will have delivered at least one major application (NDA/BLA or sNDA/sBLA).
• Experience with immunology late-stage development/marketed products ideal but not required. Other therapeutic areas will be considered.
• Great leadership skills with high emotional intelligence.
• Must be a great team player with strong verbal and written communication skills.

Skills

• Must demonstrate a firm commitment to achieving corporate objectives while maintaining the highest ethical, regulatory, and scientific standards.
• Proven track record practicing sound judgment as it relates to risk assessment.
• Highly conversant and knowledgeable of new and emerging regulations and guidance. Understanding of GMPs, GLPs, and GCPs; solid understanding of where to seek and how to interpret regulatory information.
• Fluent written and verbal communication, presentation, and facilitation skills in English.

Personal Attributes

• High ethical standards and ability to demonstrate Sobi values.
• Strong negotiation skills and significant experience in interacting with regulatory authorities.
• Risk identification and problem-solving skills.
• Actively demonstrates cross-cultural sensitivity and inclusive behavior.
• Ability to manage complex issues and coordinate multiple projects simultaneously.

Benefits

Your total compensation at Sobi goes beyond just your base salary and annual bonus. It also includes a robust suite of benefits, such as:

• A competitive 401(k) match to support your financial future.
• Tuition and wellness reimbursements to invest in your personal and professional growth.
• A comprehensive medical, dental, and vision package to prioritize your health and well-being.
• Additional recognition awards to celebrate your achievements.

Pay

The base salary range for this role is 185,000 – 210,000 USD. Each individual offer will be determined based on several factors, including your experience, qualifications, and location. Additionally, this role is eligible for both short-term and long-term bonuses, as outlined in the plan details.

All Sobi employees need to demonstrate behaviors in line with Sobi's core values: Care, Ambition, Urgency, Ownership, and Partnership.