Consultant – RWE Project Manager

Ividata Life Sciences

. Select and oversee CROs and data providers in collaboration with the Procurement and Outsourcing teams .

Posted 10/5/2026full-timeParis • FranceMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial project management, including oversight of CROs and service providers, while ensuring compliance with European regulatory standards. Proficient in monitoring project performance, timelines, and budgets, with strong analytical and proactive problem-solving skills.

Highest-signal resume keywords

Clinical Trial Project ManagementCRO ManagementEuropean Regulatory ComplianceReal-World Studies ExpertiseFluent English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project ManagementKPI MonitoringRisk AssessmentBudget ManagementData Analysis

Soft Skills

Analytical MindsetProactivityAutonomyLeadershipCommunication

Certifications & Qualifications

Pharm.D.Master’s Degree in EpidemiologyMaster’s Degree in BiostatisticsMaster’s Degree in Public HealthMaster’s Degree in Health Data Science

Industry Keywords

Trial Master FileService Provider ManagementMonitoring ReportsStudy CloseoutDocument Preparation

About the role

Key responsibilities & impact

Select and oversee CROs and data providers in collaboration with the Procurement and Outsourcing teams
Draft specifications and manage service providers
Monitor KPIs, timelines, and budgets
Identify risks, propose mitigation plans, and escalate roadblocks to the PMO Director
Ensure the quality and timely delivery of project deliverables
Ensure the Trial Master File is complete through study closeout
Lead the internal project team and coordinate project meetings
Review and approve monitoring and deviation reports
Interact directly with external sponsors to ensure the effective implementation and monitoring of studies
Contribute to document preparation, including contracts and internal protocol review
Monitor performance, timelines, and budgets
Provide management reporting

Requirements

What you’ll need

Pharm.D. or a Master’s degree specializing in Epidemiology, Biostatistics, Public Health, or Health Data Science
More than 3 years of successful experience in clinical trial project management
Strong expertise in conducting real-world studies
Experience managing CROs and service providers
Proficiency in the European regulatory environment governing real-world studies
Analytical mindset, proactivity, autonomy, and the ability to assess project feasibility
Fluent English required

Benefits

Comp & perks

Possibility of partial remote work
Stimulating and collaborative environment
High-impact assignments
Opportunities for career development alongside passionate experts
Work on projects across the pharmaceutical, biotechnology, medical device, animal health, cosmetics, and nutrition sectors