Latigo Biotherapeutics, Inc. Jobs Hiring Now
Latigo Biotherapeutics, Inc. is hiring for 16 open roles on Migrate Mate as of October 15, 2026, concentrated in clinical trials & medical research and finance. Migrate Mate updates Latigo Biotherapeutics, Inc.'s live openings daily. Latigo Biotherapeutics is a biotherapeutics company focused on developing treatments for chronic pain and related conditions, with roles spanning clinical operations, clinical pharmacology, and program leadership.
Find Latigo Biotherapeutics, Inc. JobsOverview
Latigo Biotherapeutics, Inc. hiring data on Migrate Mate, as of October 15, 2026.
- Open jobs
- 16
- Top team
- Clinical Trials & Medical Research
- Seniority
- Manager level or above
- Work type
- 44% remote or hybrid
- Top location
- San Francisco
Open Roles at Latigo Biotherapeutics, Inc.
Showing 16 of 16+ Latigo Biotherapeutics, Inc. jobs
Location: This position can be located in Thousand Oaks, CA, San Francisco Bay Area, CA or Washington, D.C. area
Overview
Reporting to the Vice President of Regulatory, the 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 and problem-solving skills.
- Attention to detail is essential.
Location: This position can be located in Thousand Oaks, CA, San Francisco Bay Area, CA or Washington, D.C. area
Overview
Reporting to the Vice President of Regulatory, the 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 and problem-solving skills.
- Attention to detail is essential.
Job Roles at Latigo Biotherapeutics, Inc.
Working at Latigo Biotherapeutics, Inc.
Latigo Biotherapeutics, Inc.'s 16 open roles are manager level or above, and about 44% are remote or hybrid. The most active teams are clinical trials & medical research, finance, and clinical support. Latigo Biotherapeutics is a biotechnology and pharmaceuticals company developing biologic therapies for chronic pain. Open positions span clinical operations, clinical pharmacology, and disease-area program leadership, reflecting an active late-phase clinical development pipeline. Most Latigo Biotherapeutics, Inc. roles are based in San Francisco and Thousand Oaks.
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Browse jobs by roleLatigo Biotherapeutics, Inc. Jobs: Frequently Asked Questions
How many jobs is Latigo Biotherapeutics, Inc. hiring for right now?
Latigo Biotherapeutics, Inc. is hiring for 16 open roles on Migrate Mate as of October 15, 2026, updated daily, concentrated in clinical trials & medical research and finance. Positions span clinical operations, clinical pharmacology, and program leadership, with most postings at manager level or above.
What kinds of roles does Latigo Biotherapeutics, Inc. hire for?
The most active teams are clinical trials & medical research, finance, and clinical support. Latigo Biotherapeutics hires for clinical operations, clinical pharmacology, and disease-area program leadership roles supporting its chronic pain pipeline. Most postings are manager level or above, reflecting a focus on experienced professionals in biopharmaceutical drug development and late-phase clinical trial management.
Are Latigo Biotherapeutics, Inc. jobs remote or in-person?
A mix of remote and on-site. About 44% of Latigo Biotherapeutics, Inc.'s open roles on Migrate Mate are remote or hybrid as of October 15, 2026, with the rest based in San Francisco. Each Latigo Biotherapeutics, Inc. listing shows its work location so you can filter before applying.
How do I apply to a job at Latigo Biotherapeutics, Inc.?
Find a role that matches your background in Latigo Biotherapeutics' listings on Migrate Mate, then follow the listing through to Latigo Biotherapeutics, Inc.'s own careers page to complete the application. Latigo Biotherapeutics manages its own hiring process directly, so all applications, follow-ups, and interview scheduling are handled by their team.
Does Latigo Biotherapeutics, Inc. hire entry-level?
Most of Latigo Biotherapeutics, Inc.'s open roles on Migrate Mate are manager level or above as of October 15, 2026. Entry-level openings are limited. Check individual Latigo Biotherapeutics, Inc. listings for stated experience requirements.
Where is Latigo Biotherapeutics, Inc. hiring?
Most Latigo Biotherapeutics, Inc. roles are based in San Francisco and Thousand Oaks, and about 44% offer remote or hybrid work as of October 15, 2026. Migrate Mate shows the location on each listing.