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Associate/Sr. Associate - Trial Capabilities - Polish - Job Opportunity at Eli Lilly

Cork, Ireland
Full-time
Mid-level
Posted: May 19, 2025
Hybrid
EUR 45,000 - 65,000 annually based on Cork market rates for clinical research roles and Eli Lilly's market position

Benefits

Comprehensive healthcare coverage with premium benefits package
Competitive pension and life assurance benefits
Flexible hybrid working arrangement with modern campus facilities
Subsidized on-site dining facilities
Professional-grade fitness center access
Transportation subsidies and convenient parking
Extensive professional development programs and educational assistance
Holistic wellbeing initiatives under 'Live Your BEST Life' program
Strong DEI programs with multiple employee resource groups

Key Responsibilities

Lead clinical trial site activation and management processes with direct accountability for regulatory compliance
Drive strategic partnerships with investigator sites through documentation, budget negotiation and operational oversight
Ensure inspection readiness through comprehensive Trial Master File management
Coordinate with regulatory authorities and ethics review boards for trial approvals
Manage site performance tracking and compliance monitoring
Execute risk management and issue resolution for trial operations
Implement data privacy and country-specific regulatory requirements
Drive continuous process improvement through knowledge sharing and best practices

Requirements

Education

Bachelor's degree preferably in a scientific or health related field

Experience

Two years clinical research experience or relevant experience preferred

Required Skills

Clinical development understanding Project management expertise Compliance environment knowledge Communication and negotiation skills Problem-solving capabilities Self-management abilities Organizational skills Fluency in English and Polish
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Sauge AI Market Intelligence

Industry Trends

Increasing focus on decentralized clinical trials requiring enhanced site management capabilities and digital coordination skills Growing importance of data privacy and regulatory compliance in multinational clinical research Shift towards more complex trial designs demanding greater site coordination expertise Rising demand for bilingual clinical research professionals due to expanding global trial networks

Role Significance

Typically part of a 10-15 person trial capabilities team, collaborating with broader clinical operations department of 50-100 professionals
Mid-level position with significant operational autonomy and direct impact on clinical trial execution efficiency

Key Projects

Multi-center clinical trial coordination across multiple European sites Regulatory submission management for new trial approvals Site performance optimization initiatives Clinical trial documentation system implementations

Success Factors

Strong understanding of clinical research regulatory frameworks and GCP guidelines Excellent stakeholder management abilities across multiple cultural contexts Proven track record in clinical trial documentation and site management Ability to navigate complex organizational structures and drive results through influence

Market Demand

High demand position due to expanding clinical trial activities in Eastern European markets and increasing need for Polish language capabilities in global trials

Important Skills

Critical Skills

Bilingual proficiency (English/Polish) is essential for effective site communication and document management Clinical research expertise for ensuring trial compliance and quality Project management capabilities for coordinating multiple site activities Regulatory knowledge for ensuring compliance across different jurisdictions

Beneficial Skills

Experience with electronic trial master file systems Understanding of pharmacovigilance processes Knowledge of clinical data management systems Familiarity with risk-based monitoring approaches

Unique Aspects

Opportunity to work with Polish market while based in Ireland, offering unique cross-cultural exposure
Access to cutting-edge clinical trial management systems and processes
Strong focus on employee development and internal mobility
Robust DEI initiatives with four established employee resource groups

Career Growth

2-3 years in role before advancement opportunity, with potential fast-track progression based on performance and business need

Potential Next Roles

Clinical Operations Manager Senior Trial Manager Regional Clinical Research Lead Clinical Project Manager

Company Overview

Eli Lilly

Eli Lilly is a leading global pharmaceutical company with a strong focus on innovative drug development and significant investment in R&D

Top-tier pharmaceutical company with robust clinical research infrastructure and competitive compensation packages
Cork location serves as a strategic hub for European operations with over 2000 employees across various functions
Strong emphasis on professional development, work-life balance, and inclusive workplace practices with significant investment in employee wellbeing
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