Senior Director, Regulatory Affairs

Latigo Bio; Thousand Oaks (CA); Presencial; USD 260.000 - 360.000; Jornada completa

Descripción de la vacante

Latigo Bio is seeking a Senior Director of Regulatory Affairs to lead regulatory strategy and execution across development programs, ensuring compliance with FDA, EMA and other authorities.

You will oversee INDs, CTAs, NDAs, and briefing documents, manage regulatory vendors, and guide cross-functional teams from discovery through commercialization. This role supports US and international filings and requires strong communication, risk management, and a track record in small molecules.

Formación

• Bachelor’s, Master’s, PharmD, or PhD in life sciences.
• Minimum of 8 years of Regulatory experience.
• Direct experience leading/supporting FDA interactions.
• Experience with IND submissions.
• US registration experience ideal.
• Experience with small molecules and pain area preferred.
• Excellent written and verbal communication skills.
• Attention to detail and strong analytical skills.

Responsabilidades

• Lead regulatory strategies to support product development.
• Coordinate FDA/EMA interactions and regulatory meetings.
• Oversee IND/CTAs/NDAs submission quality.
• Ensure timely, compliant regulatory documents.
• Collaborate with Clinical, CMC, Quality, and leadership teams.
• Provide regulatory input to study designs and labeling.

Conocimientos

Regulatory leadership

FDA interactions

US regulatory procedures

IND submission

Cross-functional collaboration

Regulatory project management

Regulatory strategy

Documentation & submissions

Attention to detail

Analytical problem-solving

Educación

Bachelor's degree in life sciences

Master's degree

PharmD

PhD

Descripción del empleo

Location:

This position can be located in Thousand Oaks, CA, San Francisco Bay Area, CA or Washington, D.C. area

Overview:

Reporting to the Senior Vice President of Regulatory, the Senior Director of Regulatory Affairs will support regulatory strategy and lead regulatory execution for the company’s development programs, ensuring compliance with global health authority requirements (FDA, EMA, and other regulatory agencies). This role will be responsible for developing and implementing regulatory activities to support the clinical development plans including leading submissions, managing regulatory vendors, support of regulatory interactions, and providing regulatory guidance to cross-functional teams.

Responsibilities:

Regulatory Strategy & Leadership

• Lead execution and implementation of regulatory strategies to support product development.
• Support regulatory interactions with global health authorities, including FDA, EMA, MHRA, and others.
• Provide regulatory input into clinical development plans, study designs, labeling strategies etc.
• Anticipate and mitigate regulatory risks; develop contingency plans as needed.

Submissions & Compliance

• Oversee the preparation, review, and submission of high-quality regulatory documents (INDs, CTAs, NDAs, briefing documents, etc.).
• Ensure timely regulatory submissions are complete and accurate.
• Maintain current knowledge of applicable regulatory requirements and ensure organizational compliance.
• Lead/support preparation and management of regulatory meeting requests and briefing documents for FDA Type B/C meetings and equivalent ex-US interactions.

Cross-Functional Collaboration

• Partner with Clinical Development, CMC, Nonclinical, Quality, and leadership teams to integrate regulatory considerations.
• Provide regulatory guidance on study protocols, statistical analysis plans, and clinical trial conduct.
• Quality mindset regarding CMC submissions and inspections.

Requirements:

• Bachelor's, Master's, PharmD, or PhD, preferably in life sciences
• Minimum of 8 years of Regulatory experience
• Direct experience leading/supporting FDA interactions
• Ability to oversee regulatory activities and manage processes from research/discovery, CMC, and clinical and manage process from clinical development through to commercialization planning
• US registration experience ideal
• Experience with small molecules and pain (or similar area) is preferred
• Experienced with IND submission and maintenance
• Knowledge of US procedures (fast to market procedures would be an advantage)
• Familiarity with EU CTA/MAA regulatory processes preferred
• Regulatory Project Management experience preferred
• Excellent written and verbal communication skills
• Must display strong analytical andproblem-solving skills.
• Attention to detail is essential.