Consultant, Clinical Project Manager

Jobtailor; Paris; Sur place; EUR 70 000 - 95 000; Plein temps

Résumé du poste

Jobtailor seeks an experienced Clinical Project Manager to oversee international Phase I–IV trials and real-world evidence projects. You will lead cross-functional teams across CRAs, CTMs, and country project managers, coordinating with CROs and global Medical Affairs, Data Management, and Biostatistics teams.

The role requires 3–5 years in clinical project management, strong knowledge of GCP/ICH, and excellent organizational and communication skills to operate in a matrix environment.

Qualifications

• 3–5 years of experience in clinical project management
• Experience managing international, multi-country studies
• Fluent English required for leading meetings and documentation
• GCP knowledge and regulatory compliance
• Strong organizational and interpersonal skills

Responsabilités

• Operationally manage international Phase I–IV clinical trials
• Manage real-world evidence projects from set-up through closeout
• Lead local and central teams including CRAs, CTMs, and country PMs
• Manage international CROs
• Coordinate with global Medical Affairs, Data Management, and Biostatistics teams
• Ensure compliance with GCP, ICH, FDA/EMA requirements
• Manage study timelines and budgets
• Monitor performance and quality indicators
• Collaborate with clients in pharmaceutical and biotech sectors

Connaissances

Clinical Project Management

GCP

ICH Regulations

International Multi-Country Studies

Fluent English

Organizational Skills

Interpersonal Skills

Formation

PharmD/PhD/MSc in science

Clinical research specialization preferred

Outils

CROs

Data Management Systems

Biostatistics Tools

Description du poste

• Operationally manage international Phase I-IV clinical trials
• Manage real-world evidence (RWE) projects from set-up through closeout
• Lead local and central teams, including Clinical Research Associates (CRAs), Clinical Trial Managers (CTMs), and country project managers
• Manage international Contract Research Organizations (CROs)
• Maintain ongoing coordination with global Medical Affairs, Data Management, and Biostatistics teams
• Ensure compliance with Good Clinical Practice (GCP), ICH regulations, and local and international regulatory requirements
• Manage study timelines and budgets
• Monitor performance and quality indicators
• Collaborate with clients in the pharmaceutical and biotechnology sectors

Requirements

• Doctor of Pharmacy (PharmD), PhD, or Master's degree in a scientific discipline
• Specialization in clinical research preferred
• At least 3-5 years of experience in clinical project management
• Proven experience managing international, multi-country studies
• Fluent or bilingual English required for leading meetings and preparing documentation on a daily basis
• Excellent organizational, attention-to-detail, and forward-planning skills
• Strong interpersonal skills to succeed in a matrix management environment
• Knowledge of and compliance with Good Clinical Practice (GCP)
• Knowledge of ICH regulations and FDA and EMA regulatory requirements

Core Competencies

Demonstrates expertise in managing international clinical trials and real-world evidence projects, ensuring compliance with Good Clinical Practice (GCP) and ICH regulations. Proven ability to lead cross-functional teams and manage study timelines and budgets effectively.

Highest-signal resume keywords

• Clinical Project Management
• Good Clinical Practice (GCP)
• ICH Regulations
• International Multi-Country Studies
• Fluent English

ATS Optimization Keywords

Hard Skills

• Clinical Trial Management
• Real-World Evidence (RWE) Management
• Study Timeline Management
• Budget Management
• Performance Monitoring

Soft Skills

• Organizational Skills
• Attention to Detail
• Interpersonal Skills
• Forward Planning

Industry Keywords

• Pharmaceutical Sector
• Biotechnology Sector
• FDA Regulatory Requirements
• EMA Regulatory Requirements

Tools & Technologies

• Clinical Research Organizations (CROs)
• Data Management Systems
• Biostatistics Tools