Global Study Manager

ICON plc

Senior Clinical Trial Manager handling clinical trial operations at ICON. Overseeing budgets and mentoring CRAs for high-quality clinical programme outcomes.

Posted 7/10/2026full-timeRemote • 🇧🇬 BulgariaSeniorLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Trial Management, including oversight of trial operations, budget management, and team development. Proven ability to drive enrollment, mentor Clinical Research Associates, and foster relationships with stakeholders to ensure successful trial outcomes.

Highest-signal resume keywords

Clinical Trial ManagementBudget OversightTeam MentoringStudy Start-Up ActivitiesMonitoring Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial OperationsMonitoring Plans DevelopmentResource AllocationCorrective Action PlansDatabase Lock ManagementEnrollment StrategiesTrial Component ManagementPerformance Optimization

Soft Skills

Stakeholder Relationship ManagementTeam CoordinationProblem Solving

Industry Keywords

CROPharmaceutical OrganizationClinical Research AssociatesGlobal TrialsHealth SciencesLife Sciences

About the role

Key responsibilities & impact

Manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.
Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.
Oversee the clinical portion of the budget to ensure efficient resource allocation.
Develop monitoring plans and tools, ensuring effective study oversight.
Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
Drive enrollment and lead study start-up activities, adhering to timelines.
Review trip reports and implement corrective and preventative action plans when necessary.
Foster productive relationships with Sponsors, vendors, and cross-functional teams.

Requirements

What you’ll need

A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization
Bachelor's degree in health, life sciences, or other relevant fields of study
At least 10+ years of relevant experience in clinical trial management
2+ years of monitoring experience preferred
Experience in managing complex or global trials is advantageous
Experience in managing all trial components from start-up to database lock preferred
Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives preferred
Willingness to travel as required (approximately 25%)

Benefits

Comp & perks

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways