Senior Manager – Clinical Trial Liaison

Regeneron

. Manage day-to-day operational oversight for delivery of defined therapeutic areas/projects within the Americas region for the Clinical Trial Liaison team .

Posted 10/16/2026full-timeRemote • United StatesSenior💰 $134,400 - $219,200 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in global clinical trial operations, including managing field-based Clinical Trial Liaison teams and ensuring compliance with ICH GCP and regional regulatory requirements. Proven ability to build relationships with investigators and site staff while effectively overseeing performance metrics and operational strategies.

Highest-signal resume keywords

Clinical Trial Operations ManagementPeople Management ExperienceICH GCP CompliancePerformance ManagementRelationship Building

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial LiaisonOperational Strategy ImplementationPerformance OversightResource PlanningPatient RecruitmentSite IdentificationRegulatory ComplianceTraining Needs AssessmentPerformance Metrics AnalysisScientific Knowledge

Soft Skills

Excellent CommunicationInterpersonal SkillsOrganizational SkillsCollaborative Working StyleCoaching and Mentoring

Industry Keywords

Clinical Development ProcessCRO ExperienceField-Based TeamsCross-Cultural AwarenessBusiness English Fluency

About the role

Key responsibilities & impact

Manage day-to-day operational oversight for delivery of defined therapeutic areas/projects within the Americas region for the Clinical Trial Liaison team
Manage and oversee the performance of field-based CTLs and CTL staff provided by third-party FSP vendors
Implement and execute portfolio-wide operational strategy for assigned therapeutic areas
Build relationships with investigators and investigator site staff
Identify potential new investigators to support optimal placement of clinical trials
Provide input in cross-functional forums on study, program, and operational strategies
Conduct line management and performance oversight of assigned CTLs, including goals, deliverables, metrics, reviews, and development planning
Support resource planning and capacity recommendations
Monitor FSP CTL performance against service-level agreements and escalate concerns
Ensure CTL execution of study deliverables, including feasibility, site identification and selection, patient recruitment, and retention
Identify process improvements and advocate for the CTL team
Maintain relationships with internal stakeholders and the external investigator community
Participate in remote and onsite co-visits with CTLs at investigator sites for coaching, oversight, and clinical trial execution
Act as the first escalation point for internal study teams, sites, and CRO partners
Support CTL attendance at investigator meetings
Produce monthly performance summaries for the Regional Head
Work with Medical Affairs/Field Medical teams to support CTLs in local meetings
Support CTLs in regulatory GCP inspections and/or audits as sponsor representative
May work up to 15% as a CTL on studies and with sites
Support onboarding, identify training needs, and ensure consistent role, study, systems, and compliance training across CTLs

Requirements

What you’ll need

Bachelor's degree as a minimum
Master's/Ph.D./PharmD. degree preferred
Minimum 8 years of relevant industry and/or CRO experience in clinical trial operations
At least 3 years in a people management role with direct line management accountability
Demonstrated line and performance management experience, including formal performance reviews and development planning
Extensive experience in global clinical trial operations
Track record of managing and developing field-based teams
Extensive scientific knowledge and understanding of the clinical development process, including ICH GCP and regional regulatory requirements
Excellent communication of technical and scientific information
Excellent interpersonal skills and collaborative and independent working style
Ability to build effective relationships with principal investigators and site staff
Strong organizational skills with effective time use and prioritization
Cross-cultural awareness
Fluent in Business English
Strong operational Clinical Trial Liaison experience with consistent and excellent performance metrics
Coaching and mentoring experience

Benefits

Comp & perks

Annual bonuses or other incentive plans
Equity awards
Pension or retirement benefits
401(k) company match
Health and wellness programs
Fitness centers
Medical, dental, vision, life, and disability insurance benefits
Paid time off
Family support benefits
Reasonable accommodation during the recruitment process where required
Inclusive workplace culture