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Korro Bio, Inc.

Senior Clinical Trial Manager

Korro Bio, Inc.

. Plan, drive, and oversee all aspects of multicenter global clinical trials in compliance with GCPs, SOPs, designated budgets, and timelines .

Posted 9/15/2026full-timeCambridge • Massachusetts • United StatesSenior💰 $163,333 - $186,667 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates extensive experience in managing multicenter global clinical trials, ensuring compliance with GCPs and regulatory requirements while optimizing trial design and execution. Proven ability to lead cross-functional teams and manage clinical budgets effectively.

Highest-signal resume keywords
Clinical Operations LeadershipGlobal Regulatory ComplianceClinical Trial ManagementCross-Functional Team LeadershipClinical Data Analysis

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial DesignProtocol ReviewCase Report Form DesignAdverse Event ReportingClinical MonitoringData Integrity AssuranceBudget ManagementRisk-Based OversightStudy DocumentationPatient Accrual Tracking
Soft Skills
Strategic ThinkingVerbal CommunicationWritten CommunicationLeadership SkillsPersuasive Communication
Tools & Technologies
Clinical Trial Management SystemsElectronic Data Capture SystemsTrial Master File Management
Industry Keywords
Good Clinical PracticeClinical DevelopmentRare DiseasesFirst-In-Human StudiesGlobal Clinical StudiesICH Guidelines

About the role

Key responsibilities & impact
  • Plan, drive, and oversee all aspects of multicenter global clinical trials in compliance with GCPs, SOPs, designated budgets, and timelines
  • Drive implementation of clinical operational strategy for assigned clinical studies
  • Optimize trial design and execution and collaborate with study teams to accelerate clinical trial timelines
  • Manage CROs and vendors, including contracting and clinical budgets
  • Develop contingency plans for clinical trials
  • Coordinate and lead study team meetings and update the Program Team on timelines and milestones
  • Contribute to study documentation, including protocol review, study plans, ICFs, and CRF design
  • Participate in CRO/vendor identification, qualification, and selection
  • Participate in site selection; review consent forms; track patient accrual and study progress; assure patient eligibility; document protocol deviations/violations; and manage adverse event reporting
  • Oversee clinical monitoring from site qualification through site closure
  • Assure clinical data integrity through review of case report forms, source documents, and medical records
  • Evaluate and analyze clinical data
  • Oversee CRO delivery of studies in alignment with timelines and budgets
  • Establish transparent communication, clear goals, and risk-based oversight
  • Ensure compliance with internal policies, GCPs, and applicable regulations; maintain inspection readiness
  • Oversee vendor contracts and clinical study budgets; report progress to Finance
  • Provide input to Clinical Study Reports and Investigator Brochures, including data cleaning, listing review, and report writing
  • Oversee TMF management and review TMF documentation
  • Travel to field sites as needed, under 25%

Requirements

What you’ll need
  • Bachelor’s Degree; Life Sciences preferred
  • 8+ years of relevant clinical development and operations experience in clinical operations leadership roles
  • Experience leading global clinical studies/programs, with track records of initiating and delivering early phase trials
  • Experience in rare diseases and early phase studies, including FIH studies, highly desirable
  • Strong leadership skills driving large cross-functional teams
  • Deep knowledge of global regulatory and compliance requirements for clinical research, local country requirements, and ICH GCP
  • Experience with global regulatory inspections
  • Excellent critical and strategic thinking
  • Global clinical operations and development experience across therapeutic areas
  • Demonstrated ability to rapidly learn new indications
  • Excellent verbal and written communication skills
  • Ability to persuasively convey ideas and data

Benefits

Comp & perks
  • Equity-based compensation
  • Medical insurance
  • Dental insurance
  • Vision insurance
  • 401(k) retirement plan
  • Life insurance
  • Dependent care flexible spending account
  • Company-funded health savings account
  • Free parking
  • Hybrid work arrangement