Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Excelya

Global Clinical Project Manager

Excelya

. Lead and coordinate the operational conduct of international clinical studies .

Posted 10/17/2026full-timeParis • FranceMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing international clinical studies, ensuring compliance with ICH-GCP guidelines, and overseeing project timelines, budgets, and stakeholder relationships. Proven ability to lead cross-functional teams and implement risk mitigation strategies for successful study delivery.

Highest-signal resume keywords
Clinical Project ManagementICH-GCP ComplianceStakeholder ManagementBudget ManagementOncology Clinical Studies

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Study CoordinationStudy Timeline ManagementRisk Identification and MitigationPatient Recruitment MonitoringStudy Reporting
Soft Skills
Excellent CommunicationLeadership Skills
Industry Keywords
International Clinical TrialsCRO ManagementQuality ObjectivesContinuous Process ImprovementPediatric Clinical Studies

About the role

Key responsibilities & impact
  • Lead and coordinate the operational conduct of international clinical studies
  • Oversee study timelines, milestones, budget, and quality objectives
  • Manage relationships with investigational sites, CROs, vendors, and study stakeholders
  • Ensure compliance with ICH-GCP, regulatory requirements, and study procedures
  • Monitor study progress, patient recruitment, and site performance
  • Identify risks and implement mitigation plans to ensure successful study delivery
  • Coordinate cross-functional teams and facilitate project governance meetings
  • Contribute to study reporting, inspection readiness, and continuous process improvement

Requirements

What you’ll need
  • Degree in Life Sciences, Pharmacy, Medicine, or related field
  • Significant experience in Clinical Project Management within clinical research
  • Strong knowledge of international clinical trials and ICH-GCP guidelines
  • Experience managing CROs, vendors, budgets, and study timelines
  • Previous exposure to oncology and/or pediatric clinical studies is highly desirable
  • Excellent communication, stakeholder management, and leadership skills
  • Fluent in English

Benefits

Comp & perks
  • Opportunity to contribute to innovative research programs with global impact
  • Highly collaborative environment
  • Inclusive environment supporting collaboration and individual growth
  • Diverse and stimulating projects
  • Opportunities to collaborate with leading experts
  • Environment that values natural talents, encourages boldness, pushes boundaries, and cultivates potential
  • Employee experience-focused culture
  • Opportunity to contribute to scientific, operational, and human knowledge
  • Mission focused on improving the patient journey