Latigo Biotherapeutics, Inc.
Director, Regulatory Affairs
Latigo Biotherapeutics, Inc., Thousand Oaks, California, United States, 91362
Location
This position can be located in Thousand Oaks, CA or the San Francisco Bay Area Company Description
Latigo Biotherapeutics, Inc.
is a private, early-stage clinical biotechnology company focused on discovering and developing the next generation of non-opioid medicines for pain and pain-related syndromes. Our mission is the development of novel therapies that transform the lives of patients. The company headquarters are in Thousand Oaks, CA and has a highly successful management team as well as an experienced Board of Directors. At Latigo, we value science, patient-focus, and innovation. Position Overview
Reporting to the Vice President of Regulatory, the Director, 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 Office based – minimum 3 days weekly 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 and problem-solving skills. Attention to detail is essential.
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This position can be located in Thousand Oaks, CA or the San Francisco Bay Area Company Description
Latigo Biotherapeutics, Inc.
is a private, early-stage clinical biotechnology company focused on discovering and developing the next generation of non-opioid medicines for pain and pain-related syndromes. Our mission is the development of novel therapies that transform the lives of patients. The company headquarters are in Thousand Oaks, CA and has a highly successful management team as well as an experienced Board of Directors. At Latigo, we value science, patient-focus, and innovation. Position Overview
Reporting to the Vice President of Regulatory, the Director, 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 Office based – minimum 3 days weekly 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 and problem-solving skills. Attention to detail is essential.
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