Clinical Research Manager – Local Trial Manager

Job not on LinkedIn

🔥 0 minutes ago

🇫🇷 France – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Lead end-to-end performance and project management of assigned clinical trial protocols • Manage study start-up activities, including site selection strategies, monitoring plans, and trial planning tools • Review and contribute to patient recruitment and retention strategies • Provide leadership, guidance, and direction to project team members across multiple locations and functions • Evaluate project resource requirements and monitor resource utilization throughout the study lifecycle • Address and resolve site issues, escalating risks and ensuring timely closure • Monitor study timelines, patient recruitment, retention, and data cleaning activities • Maintain oversight of quality standards and follow up on quality-related issues • Drive process improvements to enhance study efficiency and operational performance • Contribute to revenue recognition forecasting and project planning activities • Collaborate on database lock activities and study close-out deliverables • Ensure completion of administrative close-out procedures, study archiving, and client documentation requirements • Manage complex oncology clinical trials for a pharmaceutical client • Ensure compliance with ICH-GCP, local regulations, client requirements, and quality standards

🎯 Requirements

• Degree in a life science, nursing qualification, or relevant clinical and/or clinical management experience • Substantial experience in clinical research, including relevant experience as a team leader in clinical functions or proven experience coordinating clinical trials • Knowledge of ICH-GCP, regulatory requirements, SOPs, and clinical trial processes • Experience managing clinical trial activities, study operations, site oversight, and vendor relationships • Strong leadership, stakeholder management, and project coordination skills • Ability to collaborate across cross-functional and global teams • Strong communication, organization, leadership, negotiation, and problem-solving skills • Strong command of written and spoken English • Comfort working with clinical trial systems, study management processes, and project planning tools • Previous experience as a Clinical Research Associate (CRA) (preferred) • Experience in oncology clinical trials (preferred) • Experience within a pharmaceutical company, healthcare organization, or contract research organization (preferred) • Knowledge of project management methodologies and clinical study lifecycle management (preferred)

🏖️ Benefits

• Medical Plan • Life Assurance • Pension • Comprehensive benefits package for eligible employees • Additional benefit offerings in accordance with the terms of applicable plans • Home-based work capacity in France • Leadership opportunities • Continuous development • Career progression opportunities