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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 fitCore Competencies
Use this summary to align your resume positioning with the role.
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
Tailor your resumeApplicant 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