Clinical Research Manager – Local Trial Manager

This is a fully remote position, open to applicants in France.

📋 Description

• Oversee the complete performance and project management of designated clinical trial protocols.

• Manage the initiation activities of the study, which include strategies for site selection, monitoring plans, and tools for trial planning.

• Review and actively contribute to strategies aimed at patient recruitment and retention.

• Provide leadership, direction, and guidance to project team members spread across various locations and functions.

• Assess project resource needs and keep track of resource utilization throughout the study's lifecycle.

• Address site-related issues, escalate risks, and ensure timely resolutions.

• Monitor timelines of the study, patient recruitment, retention, and data cleaning processes.

• Maintain oversight of quality standards and follow up on any quality-related concerns.

• Drive process enhancements to improve study efficiency and operational performance.

• Assist in revenue recognition forecasting and project planning tasks.

• Collaborate on activities related to database lock and deliverables for study close-out.

• Ensure all administrative close-out procedures, study archiving, and client documentation requirements are completed.

• Manage intricate oncology clinical trials for a pharmaceutical client.

• Ensure adherence to ICH-GCP, local regulations, client requirements, and quality standards.

⛳️ Requirements

• A degree in a life science, nursing qualification, or relevant clinical and/or clinical management experience is required.

• Extensive experience in clinical research, including relevant experience leading a team in clinical functions or proven coordination of clinical trials.

• Familiarity with ICH-GCP, regulatory standards, SOPs, and processes related to clinical trials.

• Experience in managing activities related to clinical trials, study operations, site supervision, and vendor relations.

• Strong skills in leadership, stakeholder management, and project coordination.

• Ability to work collaboratively with cross-functional and global teams.

• Excellent communication, organizational, leadership, negotiation, and problem-solving abilities.

• Proficient command of both written and spoken English.

• Comfortable utilizing clinical trial systems, study management processes, and project planning tools.

• Previous experience as a Clinical Research Associate (CRA) is preferred.

• Experience in oncology clinical trials is preferred.

• Background in a pharmaceutical company, healthcare organization, or contract research organization is preferred.

• Understanding of project management methodologies and clinical study lifecycle management is preferred.

🏝️ Benefits

• Medical Plan

• Life Assurance

• Pension

• Comprehensive benefits package for eligible employees

• Additional benefit offerings as per the terms of applicable plans

• Home-based work capacity in France

• Leadership opportunities

• Continuous development

• Opportunities for career progression