Clinical Supply Chain Therapeutic Area Project Manager

Proclinical Staffing; Dreux; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading life sciences recruitment agency is seeking a Clinical Supply Chain Project Manager in France to oversee the supply of investigational medicinal products for clinical trials. The ideal candidate will manage project scope and timelines, lead teams, and promote compliance with Good Manufacturing Practices. A postgraduate degree and proficiency in both French and English are essential. Join a dynamic team committed to advancing innovative treatments.

Qualifications

• Background in pharmacy, engineering, or a related field.
• Experience handling large and complex clinical trials.
• Familiarity with regulatory requirements and clinical supply chain processes.

Responsabilités

• Lead cross-functional teams to set up and maintain clinical study supply chains.
• Define project scope, objectives, and comprehensive plans.
• Monitor project performance, assess risks, and implement mitigation plans.

Connaissances

Project management skills

Proficiency in French and English

Communication and networking abilities

Organizational skills

Formation

Postgraduate degree in health industry

Description du poste

Overview

Proclinical is seeking a Clinical Supply Chain Project Manager to join a dynamic team dedicated to ensuring the seamless supply of investigational medicinal products (IMPs) for clinical trials. In this role, you will play a pivotal part in defining supply chain strategies, coordinating cross-functional teams, and contributing to continuous improvement initiatives. This position offers an opportunity to work in a collaborative, global environment focused on advancing innovative treatments.

Responsibilities

• Lead cross-functional teams to set up and maintain clinical study supply chains, ensuring alignment with trial milestones and timelines.
• Define project scope, objectives, and comprehensive plans to ensure timely supply and avoid stockouts.
• Collaborate with regulatory and CMC teams to align strategies and manage submissions.
• Monitor project performance, assess risks, and implement mitigation plans as needed.
• Design IMP kits, manage labeling processes, and maintain detailed project documentation.
• Regularly review and update clinical study forecasts in collaboration with relevant stakeholders.
• Address changes in study protocols, patient recruitment, and site additions, ensuring updated forecasts are consolidated.
• Manage quality events, deviations, and change controls in line with KPIs.
• Actively participate in lessons learned exercises and contribute to continuous improvement projects.
• Promote compliance with Good Manufacturing Practices (GMP) and corporate social responsibility (CSR) initiatives.

Skills & Requirements

• Background in pharmacy, engineering, or a related field, with a postgraduate degree in the health industry.
• Proficiency in French and English.
• Strong project management skills, with experience handling large and complex clinical trials.
• Excellent communication and networking abilities.
• Ability to work effectively in a matrixed, global environment.
• Strong organizational skills and a proactive approach to problem-solving.
• Familiarity with regulatory requirements and clinical supply chain processes.

Apply Now

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Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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