CCQM

Overview

Our FSPx department is expanding, and we are looking for an experienced Quality Control Manager to join our team. In this highly visible role, you will act as a trusted quality partner to our Client , ensuring that clinical trials are conducted in full compliance with GCP, regulatory requirements, and internal quality standards , while actively contributing to process improvement and inspection readiness. This position offers the opportunity to combine hands‑on clinical expertise, quality leadership, and cross‑functional collaboration in an international environment. This role is for upcoming future opportunities that may arise at Fortrea

Your Role And Responsibilities

As Quality Control Manager, you will be responsible for (but not limited to):

• Lead the development, monitoring, coordination, and execution of the annual country‑specific Quality Control (QC) plan
• Oversee the implementation and follow‑up of QC activities, ensuring alignment with Client expectations and regulatory standards
• Take ownership of Client Corrective and Preventive Actions (CAPA) arising from GCP audits and health authority inspections
• Manage and/or co‑lead key Client quality initiatives, contributing to inspection readiness and continuous improvement
• Act as a quality expert and advisor, supporting clinical teams with GCP compliance, risk mitigation, and proactive quality oversight
• Ensure adherence to current Client processes and procedures, while identifying opportunities to enhance and optimize ways of working
• Collaborate closely with cross‑functional stakeholders (Clinical Operations, Quality, Project Management, Client representatives) in a matrix environment

Experience & Qualifications

We are looking for a senior clinical research professional who brings:

• Minimum 6–8 years of clinical research monitoring experience
• Demonstrated experience leading cross‑functional teams or working in complex matrix environments
• Excellent site monitoring skills and a strong understanding of GCP requirements
• Excellent study site management capabilities, with the ability to assess risk and quality proactively
• Proven experience working with audits, inspections, and CAPAs (direct responsibility preferred)
• Excellent verbal and written communication skills in French and English
• Strong analytical, organizational, and stakeholder‑management skills
• A pragmatic, solution‑oriented mindset with a continuous improvement approach

Work environment & travel

• Willingness to travel up to 40%, including overnight stays, depending on project and country requirements
• Ability to drive and valid driver’s license required
• Flexible working environment within an FSP model, with close Client interaction

Why join us?

• Be part of a high‑impact FSPx environment, working closely with a global pharmaceutical Client
• Play a key role in clinical quality, compliance, and inspection readiness
• Combine expert‑level individual contribution with visible leadership and influence
• Work in an international, collaborative, and professional setting where quality truly matters

Learn more about our EEO & Accommodations request here.