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New · posted Oct 15

Korro Bio · Biotechnology

Associate Director, Clinical Quality Assurance

  • Cambridge, MA
  • Hybrid
  • Full-time
  • Director
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Pay$190K–$220Ka year · employer provided
EmploymentFull-time
LocationCambridge, MAHybrid
LevelDirector
FunctionQuality AssuranceQuality
Deadline

Open until filled

The role

The Associate Director, Clinical QA will provide hands-on quality oversight of Korro Bio's clinical and nonclinical programs, ensuring that studies are conducted, and that data is generated and reported in compliance with Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Clinical Laboratory Practice (GCLP). A central part of this role is planning and conducting audits of contract research organizations (CROs), laboratories, and other service providers, as well as audits of investigator sites, both in the US and internationally. This is an individual contributor role within a lean QA team, well suited to someone who enjoys a small-company environment and is equally comfortable leading an audit in the field and serving as the quality partner to study teams. The role calls for sound, risk-based judgment and a practical approach to protecting patient safety, participant rights, and data integrity across Korro Bio's global clinical development programs.

Korro is a biopharmaceutical company focused on developing a new class of genetic medicines for both rare and highly prevalent diseases using its proprietary RNA editing platform. Korro is generating a portfolio of differentiated programs that are designed to harness the body’s natural RNA editing process to effect a precise yet transient single base edit. By editing RNA instead of DNA, Korro is expanding the reach of genetic medicines by delivering additional precision and tunability, which has the potential for increased specificity and improved long-term tolerability. Using an oligonucleotide-based approach, Korro expects to bring its medicines to patients by leveraging its proprietary platform with precedented delivery modalities, manufacturing know-how, and established regulatory pathways of approved oligonucleotide drugs. Korro’s lead program is for Urea Cycle Disorders. Korro is based in Cambridge, Massachusetts. For more information, visit korrobio.com.

We are collaborative and united by a common mission. We are building a company with extraordinary people with an audacious vision to create transformative genetic medicines for prevalent diseases. Our values - Rewrite the future, On the Cutting Edge, Better Together, Dynamically Different, Kindness and Integrity form the fabric of the organization. They are reinforced daily and serve as key dimensions in the hiring process to help us ensure that Korro is a magnet for outstanding talent and a great place to work. Join us as we redefine what's possible in genetic medicine and work to make a lasting impact on human health.

What you need

Required Qualifications

  • Bachelor's degree in Life Sciences or related scientific discipline required.
  • Minimum of 10 years of experience in the biopharmaceutical industry or clinical research, including at least 7 years in GCP or clinical Quality Assurance, with a track record of independently leading vendor and investigator site audits.
  • Strong experience providing sponsor-side quality oversight of outsourced clinical and nonclinical studies, including CROs, laboratories, and other service providers.
  • Demonstrated experience independently planning, conducting, and reporting audits of investigator sites and GCP vendors such as CROs and clinical laboratories.
  • Experience auditing GLP nonclinical testing facilities and/or GCLP clinical or bioanalytical laboratories.
  • Working knowledge of ICH E6 (including E6(R3)), 21 CFR Parts 11, 50, 54, 56, 58, and 312, EU Clinical Trials Regulation (EU) No 536/2014, and GCLP principles.
  • Experience managing clinical quality events, including deviations, investigations, and CA-PAs.
  • Ability to travel up to 20% of the time, both domestic and international, including multi-day vendor and investigator site audits.

    • Korro offers competitive total rewards package, including equity-based compensation, and a comprehensive benefits package that includes medical, dental, vision, 401(k) retirement plan, life insurance, a dependent care flexible spending account and a Company-funded health savings account and free parking.

    Skills named in this posting

    What you'll do

  • Serve as the primary quality partner to Clinical Operations, Clinical Development, Regula-tory Affairs, Pharmacovigilance, Data Management, and Nonclinical teams, providing clear, practical guidance on GCP, GLP, and GCLP expectations throughout the study lifecycle.
  • Plan, conduct, report, and follow up on qualification, routine, and for-cause audits of GCP, GLP, and GCLP service providers, including CROs, nonclinical testing facilities, bio-analytical and central laboratories, and eClinical system providers, assessing the adequacy of audit responses, verifying CAPA effectiveness, and escalating significant or un-resolved issues to Quality leadership.
  • Plan and conduct investigator site audits selected on the basis of study risk, enrollment, protocol deviation trends, monitoring findings, and other quality signals; communicate observations to study teams and sites and drive corrective actions to closure.
  • Manage clinical and nonclinical quality events, including deviations, quality issues, investigations, CAPAs, and assessments of potential serious breaches, in partnership with study teams.
  • Support vendor selection and qualification, contribute to vendor oversight plans, and negotiate and maintain Quality Agreements (as needed) with clinical and nonclinical service providers.
  • Review key study documents from a quality perspective, such as protocols and amendments, informed consent forms, monitoring and data management plans, laboratory manuals, pharmacy manuals, GLP study plans and reports, clinical study reports, and Tri-al Master File (TMF) content.
  • Lead or support inspection readiness activities for Korro Bio, its CROs, and its investigator sites; provide support during health authority inspections and help prepare responses to inspection observations.
  • Oversee the development, implementation, and maintenance of quality systems supporting clinical trial quality and GCP, GLP, and GCLP compliance, including authoring, reviewing, and improving SOPs, work instructions, and training that are phase-appropriate and can scale as programs advance.
  • Track and trend audit findings, quality events, and vendor performance; report quality metrics and emerging risks to Quality leadership and program teams.
  • Support the clinical and nonclinical quality components of regulatory submissions and health authority interactions.

    • Pay and benefits

    $190,000 – $220,000 a year

    Employer provided
    How this compares

    • Equity-based compensation

    • Medical, dental, vision

    • 401(k) retirement plan

    • Life insurance

    • Dependent care FSA

    • Company-funded HSA

    Where you'll work

    Cambridge, MAHybridOpen in Maps (opens in a new tab)

    More jobs in Cambridge, MA

    Job intelligence

    The context around this role

    Live data · October 15, 2026

    Salary intelligence

    How the pay compares

    This role's midpoint is 2% below the US median for Quality Assurance roles at this level.

    This roleEmployer provided

    $190,000 to $220,000 a year

    Director roles in Massachusetts33 roles publishing pay

    Middle half $186,000 to $231,000, median $204,500

    Director roles in the US102 roles publishing pay

    Middle half $186,500 to $231,375, median $209,250
    Annual base pay
    Annual base payLowMedianHigh
    This role$190,000—$220,000
    Massachusetts$186,000$204,500$231,000
    All US$186,500$209,250$231,375

    This role: Korro Bio's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.

    Career trajectory

    Where this role sits in Quality Assurance

    The general path across 845 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Korro Bio's own promotion track.

    1. Earlier

      Associate & Specialist

      Often: Quality Engineer · Quality Technician

      $79K median227 open

    2. Earlier

      Senior & Principal

      Often: Quality Engineer · Senior Quality Engineer

      $123K median353 open

    3. One step back

      Manager

      Often: Manager, Quality Assurance · Quality Manager

      $153K median136 open

    4. This role

      Director

      Often: Director, Quality · Associate Director, Clinical Quality Assurance

      $209K median114 open

    5. Next step

      VP & Executive

      Often: Vice President, Quality Assurance · AVP

      $302K median15 open

    Career resources on Quality Assurance

    Skills DNA

    What this role leans on

    How many of the posting's 6 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

    GMP and compliance: 3 linesLab testing and methods: 3 linesDocumentation and SOPs: 2 linesInvestigations and CAPA: 3 linesValidation and qualification: 1 lineRegulatory submissions: 1 lineQuality systems and risk: 1 lineData and digital systems: 2 linesCollaboration and leadership: 4 linesGMPLab testingDocumentationInvestigationsValidationSubmissionsQuality systemsData systemsTeamwork
    • Collaboration and leadership4
    • GMP and compliance3
    • Lab testing and methods3
    • Investigations and CAPA3
    • Documentation and SOPs2
    • Data and digital systems2
    • Validation and qualification1
    • Regulatory submissions1
    • Quality systems and risk1

    Regulatory intelligence

    The rules behind this role

    Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

    From Regulatory News

    Manufacturing and quality coverage for this profession

    Company hiring pulse

    Korro Bio on Regulatory Jobs

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    See all 1 Korro Bio roles

    Similar Quality Assurance roles elsewhere

    Associate Director, Clinical Quality Assurance at Korro Bio

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