Associate Director / Director, Toxicology

Korrobio; Cambridge (MA); Hybrid; USD 180,000 - 260,000; Full time

Benefits offered by this job

Competitive compensation with equity‑f

Medical, dental, and vision coverage

401(k) retirement plan

Life insurance

Dependent care flexible spending

Company-funded health savings account

Free parking

Job summary

Korro Bio is seeking an Associate Director or Director of Toxicology to lead the design and execution of nonclinical safety studies for our RNA editing portfolio. You will build and advance Korro’s toxicology capabilities, with emphasis on oligonucleotide therapeutics, reporting to the Senior Director, DMPK.

You will lead GLP/non-GLP studies, collaborate with cross-functional teams, oversee CROs including APAC vendors, and mentor junior scientists to ensure rigorous safety assessments and timely

Qualifications

• PhD, DVM, or equivalent in toxicology, pharmacology, or related field; board certification strongly preferred.
• 6–10+ years of relevant industry experience in toxicology and IND-enabling programs.
• Deep knowledge of global regulatory expectations and GLP principles.
• Strong leadership, communication, and organizational skills in a fast-paced environment.

Responsibilities

• Lead the design, execution, and interpretation of GLP and non-GLP toxicology studies to support development programs.
• Serve as the toxicology SME on cross-functional program teams and contribute to strategy and decision-making.
• Develop nonclinical safety strategies for oligonucleotide therapeutics, including delivery and off-target effects.
• Oversee external nonclinical toxicology studies with CROs, including APAC collaborations; mentor junior scientists.

Skills

Leadership

Regulatory thinking

Cross-functional collaboration

Communication

Mentoring

Strategic planning

Education

PhD in toxicology or related field

Board certification (e.g., DABT)

Job description

Korro Bio is seeking a highly motivated Associate Director or Director of Toxicology to lead the design and execution of nonclinical safety studies across our RNA editing portfolio. Reporting to the Senior Director, DMPK, this individual will be a key scientific and strategic contributor responsible for building and advancing Korro’s toxicology capabilities, with an emphasis on oligonucleotide-based therapeutics.

Responsibilities

• Lead the design, execution, and interpretation of GLP and non-GLP toxicology studies to support target assessment, platform innovation initiatives, development candidate selection and regulatory submissions.
• Serve as the toxicology subject matter expert on cross-functional program teams, contributing to overall project strategy and decision-making.
• Develop and implement nonclinical safety strategies specific to oligonucleotide therapeutics, including considerations for sequence, chemistry, delivery, and off‑target effects.
• Experience designing, outsourcing, and overseeing nonclinical toxicology studies at external CROs, including international vendors; prior experience working with CROs in China (or broader APAC region) is highly desirable. Mandarin language skills are a plus, particularly for candidates with experience working with China based CROs.
• Ensure high‑quality execution of all external safety studies and timelines, including general toxicology, safety pharmacology, genetic toxicology, and immunotoxicology as needed.
• Prepare reports and presentations for internal and external audiences.
• Prepare and review regulatory documentation, including INDs, CTAs, Investigator’s Brochures, and responses to health authority queries.
• Author and/or oversee preparation of nonclinical sections for regulatory submissions across the product lifecycle, including INDs and later‑stage filings (NDA/BLA), with responsibility for Module 2 summaries, study reports, and health authority responses.
• Contribute to regulatory strategy and agency interactions, with experience with accelerated development pathways and/or rare disease programs being highly desirable.
• Represent Korro in regulatory interactions, including pre‑IND and other milestone meetings.
• Stay current on regulatory guidelines, safety assessment trends, and emerging science relevant to oligonucleotide and RNA‑based therapies.
• Mentor and develop junior scientists and contribute to a culture of scientific rigor, collaboration, and innovation.

Qualifications

• PhD, DVM, or equivalent in toxicology, pharmacology, or related field; board certification (e.g., DABT) strongly preferred.
• 6-10+ years of relevant industry experience in toxicology, with a strong track record of supporting mechanistic toxicology and IND‑enabling programs.
• Deep knowledge of global regulatory expectations, ICH guidelines, and GLP principles.
• Strong leadership, communication, and organizational skills, with the ability to work effectively in a fast‑paced, matrixed environment.
• Proven ability to influence across functions and effectively interface both internal and external stakeholders.

Preferred Qualifications

• Hands‑on experience with oligonucleotide‑based therapeutics is a plus.
• Mandarin language proficiency is a plus, particularly for candidates with experience collaborating with China based CROs.
• Familiarity with GalNAc or other delivery systems is a plus.

Benefits

• Competitive compensation with equity‑based components
• Medical, dental, and vision coverage
• 401(k) retirement plan
• Life insurance
• Dependent care flexible spending account
• Company‑funded health savings account
• Free parking