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Clinical Project Coordinator - Entry Level - Job Opportunity at Medpace

Lyon, France
Full-time
Entry-level
Posted: March 8, 2025
On-site
EUR 35,000 - 45,000 annually based on Lyon market rates for entry-level clinical research positions

Benefits

Flexible work environment with emphasis on work-life balance
Competitive compensation package aligned with CRO industry standards
Comprehensive PTO package exceeding French market averages
Structured professional development paths with clear advancement opportunities
Employee wellness programs indicating strong corporate culture
Regular team appreciation events fostering engagement

Key Responsibilities

Lead daily clinical trial management activities with direct impact on study outcomes and timeline adherence
Manage and maintain critical project documentation within CTMS to ensure regulatory compliance and study integrity
Drive cross-functional collaboration between internal teams, sponsors, and vendors to facilitate efficient study execution
Oversee Trial Master File maintenance ensuring complete regulatory compliance and audit readiness
Develop and track project timelines and enrollment metrics to optimize study progression
Facilitate and document project meetings to ensure clear communication and decision tracking

Requirements

Education

Bachelor's Degree in Life Sciences, Master's Degree preferred

Experience

Entry level - internship or clinical trials experience beneficial

Required Skills

Excellent oral and written English & French Languages communication skills Knowledge of Microsoft Office programs Excellent organisational and prioritisation skills Strong attention to detail
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Sauge AI Market Intelligence

Industry Trends

The CRO industry is experiencing substantial growth driven by increased outsourcing of clinical trials and rising R&D investments in biotech and pharma sectors Growing demand for bilingual clinical research professionals in European markets, particularly in major pharmaceutical hubs like Lyon Increasing adoption of digital clinical trial management systems requiring enhanced technical proficiency from coordinators

Role Significance

Typically part of a 5-10 person project team, working under senior clinical trial managers
Entry-level position with significant responsibility in clinical trial execution and potential for rapid advancement

Key Projects

Phase I-IV clinical trials across multiple therapeutic areas Regulatory documentation management and compliance assurance Site coordination and enrollment tracking Cross-functional team collaboration initiatives

Success Factors

Strong organizational skills with ability to manage multiple concurrent study timelines Excellence in cross-cultural communication given the international nature of clinical trials Attention to detail in regulatory documentation and data management Ability to adapt to evolving clinical trial management systems and processes

Market Demand

High demand with strong growth trajectory due to expanding clinical trial activities in France and increasing complexity of regulatory requirements

Important Skills

Critical Skills

Bilingual proficiency in English and French essential for effective communication with global stakeholders Project management capabilities fundamental for coordinating multiple study activities Detail orientation crucial for maintaining regulatory compliance and data accuracy

Beneficial Skills

Understanding of GCP and ICH guidelines Experience with electronic data capture systems Knowledge of medical terminology and therapeutic areas

Unique Aspects

Opportunity to work across multiple therapeutic areas including oncology and cardiology
Strong focus on employee development with structured career paths
Global exposure through international project teams
Stability of working with an established CRO with consistent growth

Career Growth

2-3 years in coordinator role before advancement to trial manager position with demonstrated performance

Potential Next Roles

Clinical Trial Manager Project Manager Clinical Operations Manager Clinical Research Associate

Company Overview

Medpace

Full-service CRO with comprehensive Phase I-IV clinical development capabilities and strong therapeutic expertise

Mid-sized CRO with strong market position, consistently recognized through industry awards and steady growth
Strategic location in Lyon strengthens presence in European pharmaceutical market with access to key clinical research centers
Professional environment with emphasis on career development and work-life balance, characteristic of established CROs
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