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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive knowledge in global trial operations and clinical development, with a strong focus on leading Clinical Trial Liaison teams and managing vendor relationships. Proficient in conducting feasibility assessments, site selection, and ensuring compliance with Good Clinical Practice and local regulations.
Highest-signal resume keywords
Clinical Operations ExperiencePeople Management AccountabilityGlobal Trial Operations KnowledgeGood Clinical Practice KnowledgeScientific Communication Skills
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 ManagementFeasibility AssessmentSite SelectionRecruitment StrategiesInvestigator Relationship ManagementPerformance Metrics ReportingQuality Delivery OversightIssue Resolution ProcessesAudit SupportInspection Support
Soft Skills
CollaborationIndependent WorkingOrganisationPrioritisationCross-Cultural Awareness
Industry Keywords
Clinical DevelopmentContract Research OrganisationInternational Council for HarmonisationService-Level AgreementsVendor Management
About the role
Key responsibilities & impact- Lead country-cluster operations and field-based Clinical Trial Liaison teams
- Lead Clinical Trial Liaison performance, development planning, formal reviews, goals, workload, and quality delivery
- Oversee vendor-provided staff against service-level agreements and raise performance concerns
- Implement standardised feasibility, site selection, recruitment, retention, and investigator issue-resolution processes
- Advise cross-functional forums on study, programme, country, capacity, and resource strategies
- Build investigator relationships
- Conduct remote and on-site co-visits
- Support meetings, audits, and inspections
- Report monthly metrics, standard methodologies, issues, and escalations
- Retain a 15% liaison workload
- Foster a collaborative, high-performing cluster aligned with regional standards and continuous improvement
- Collaborate with regional leaders, study teams, vendors, and investigator sites
Requirements
What you’ll need- Bachelor’s degree
- Eight years’ relevant clinical operations experience in industry or a contract research organisation
- Two to three years’ direct people-management accountability
- Extensive global trial operations, field-team leadership, and clinical development knowledge
- Knowledge of International Council for Harmonisation Good Clinical Practice and regional and local regulations
- Strong scientific communication, organisation, prioritisation, and investigator relationship skills
- Collaborative and independent working styles
- Cross-cultural awareness
- Fluent business English
- Additional languages are beneficial
- Ability to conduct remote and on-site co-visits and support meetings, audits, and inspections
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
- Insurance benefits (e.g. medical, dental, vision, life and disability)
- Paid time off
- Family support benefits
- Reasonable accommodation during the recruitment process where required
- Remote work mode
- 30–40% EU travel