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Study Operations Manager I - Job Opportunity at ICON

Remote, France
Full-time
Mid-level
Posted: April 23, 2025
Remote
EUR 55,000 - 70,000 annually based on French market rates for clinical operations roles

Benefits

Remote work flexibility offering improved work-life balance
Professional development in clinical research industry
Global exposure working with international teams
Career advancement opportunities within a leading CRO

Key Responsibilities

Strategic oversight of clinical trial operations at regional/country level with direct impact on study success
Leadership of site activation and regulatory submission processes ensuring compliance and efficiency
Cross-functional coordination of recruitment strategies driving enrollment targets
Vendor relationship management and performance optimization
Quality assurance and risk management for trial execution
Strategic communication management between global and local teams

Requirements

Education

Bachelor's degree or higher in life sciences, healthcare, or a related field

Experience

3-5+ years of experience in clinical trial operations

Required Skills

Good Clinical Practice (GCP) knowledge French regulatory requirements expertise Cross-functional coordination experience Project management skills Communication skills Problem-solving abilities Remote work proficiency Fluency in English & French
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Industry Trends

Increasing demand for decentralized trial management expertise as the industry shifts towards hybrid and virtual study models Growing emphasis on real-world evidence and adaptive trial designs requiring enhanced operational flexibility Rising importance of technology integration in clinical operations driving need for digital competency

Role Significance

Typically coordinates with 5-10 direct stakeholders and influences 20-30 extended team members across sites and vendors
Mid-level management position with significant operational autonomy and strategic input capabilities

Key Projects

Multi-site clinical trial operations management Site network development and management Regulatory compliance initiatives Performance optimization programs

Success Factors

Strong stakeholder management capabilities across cultural and organizational boundaries Excellent understanding of French healthcare system and regulatory landscape Ability to balance multiple competing priorities while maintaining quality standards Proactive risk management and problem-solving orientation

Market Demand

High demand with steady growth projected due to increasing clinical trial complexity and volume in Europe

Important Skills

Critical Skills

Regulatory knowledge combining GCP and French requirements - essential for ensuring compliance and study success Project management capabilities - fundamental for coordinating complex multi-stakeholder initiatives Bilingual proficiency - crucial for effective communication between global and local teams

Beneficial Skills

Change management experience Digital health technology familiarity Budget management expertise Quality management systems knowledge

Unique Aspects

Full remote work opportunity in an industry traditionally requiring significant on-site presence
Combination of local expertise requirement with global operational scope
Strategic position bridging global trial requirements with local implementation

Career Growth

Typical progression to senior level within 2-3 years with demonstrated success in delivery

Potential Next Roles

Senior Study Operations Manager Clinical Operations Director Program Manager Regional Trial Manager

Company Overview

ICON

ICON is a leading global CRO providing comprehensive clinical research services across multiple therapeutic areas

Top-tier global CRO with strong market position and consistent growth trajectory
Significant presence in France with established relationships with key sites and investigators
Matrix organization emphasizing collaboration, innovation, and professional development
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