Senior Clinical Project Manager

Excelya

. Lead and coordinate clinical trial activities at the local level from start-up to close-out .

Posted 10/9/2026full-timeParis • FranceSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trial activities, ensuring compliance with ICH-GCP and local regulations, and effectively coordinating with stakeholders and vendors. Proficient in tracking KPIs and operational deliverables while maintaining data accuracy and documentation compliance.

Highest-signal resume keywords

Clinical Project ManagementICH-GCP ComplianceRegulatory SubmissionsFluency in French and EnglishInterventional Trials Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical OperationsRegulatory Environment KnowledgeSite Selection and ActivationData Accuracy ManagementKPI TrackingOperational TroubleshootingPerformance MonitoringDocumentation ComplianceCorrective Action ManagementAudit and Inspection Readiness

Soft Skills

Strong Organizational SkillsEffective Communication SkillsAbility to Manage Multiple TasksCollaboration with Cross-Functional TeamsProblem-Solving Skills

Industry Keywords

Clinical TrialsPharmaCROLocal Investigational SitesEthics CommitteesStudy MeetingsPatient RecruitmentLogistics ManagementVendor RelationshipsOperational Deliverables

About the role

Key responsibilities & impact

Lead and coordinate clinical trial activities at the local level from start-up to close-out
Ensure local execution of global study plans in alignment with timelines and quality standards
Serve as the key point of contact for local investigational sites and regional stakeholders
Ensure clinical trial activities comply with local regulations, ICH-GCP, and internal SOPs
Coordinate local submissions to competent authorities and ethics committees when required
Monitor regulatory timelines and manage corrective actions
Support site selection, activation, monitoring, and close-out with CRAs and vendors
Manage relationships with local vendors, including logistics, labs, and CRO partners
Follow up on recruitment progress, performance, and site-level metrics
Collaborate with global study teams, medical affairs, regulatory affairs, and clinical operations
Participate in study meetings and provide updates on local activities, challenges, and achievements
Support risk mitigation plans and operational troubleshooting
Oversee data accuracy, query resolution, and documentation compliance
Track KPIs, patient recruitment, timelines, and operational deliverables
Contribute to audit and inspection readiness

Requirements

What you’ll need

Experience in clinical operations within pharma or CRO
Experience as Clinical Project Manager, Study Manager, or equivalent
Previous involvement in interventional trials (Phase II–IV preferred)
Solid understanding of ICH-GCP, regulatory environment, and local clinical research practices
Experience collaborating with investigators, CROs, and cross-functional teammates
Strong organizational, operational, and communication skills
Ability to manage several tasks simultaneously in a fast-paced environment
Fluency in French and English, written and spoken

Benefits

Comp & perks

Opportunity to grow through diverse and stimulating projects
Collaboration with leading experts
Contribute to scientific, operational, and human knowledge
Environment valuing natural talents and encouraging boldness
Opportunities to develop and contribute to the shared mission
Employee experience focus
Work with a young and ambitious healthcare company and a 900-person team