Senior Clinical Trial Assistant - Sponsor-Focused Ops

IQVIA Inc; Brussel Hoofdstad; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

IQVIA is seeking an experienced Senior Clinical Trial Assistant to support delivery of clinical research projects in a dynamic, collaborative environment. The role focuses on coordination, maintenance, and oversight of essential trial documentation to ensure regulatory compliance and on-time study milestones.

You will work with cross-functional study teams, manage study documentation, and provide guidance to junior staff, contributing to process improvements and high-quality trial conduct across

Competenze

• 2+ years of experience in clinical research.
• Strong organizational and documentation skills.
• Experience with study documentation and tracking systems.
• Knowledge of ICH-GCP.
• Fluent in Dutch/French and English.

Mansioni

• Support study documentation management and tracking systems.
• Ensure accuracy and quality of trial records through the study lifecycle.
• Coordinate study activities with clinical operations teams.
• Assist with document preparation, filing, and quality control.
• Support regulatory compliance with SOPs and GCP.
• Provide guidance to junior team members as needed.
• Participate in process improvements to boost efficiency.

Conoscenze

Clinical trial experience

Documentation management

Communication skills

Multitasking

Attention to detail

Strumenti

Microsoft Office

Descrizione del lavoro

IQVIA is seeking an experienced Senior Clinical Trial Assistant to support delivery of clinical research projects in a dynamic, collaborative environment. The role focuses on coordination, maintenance, and oversight of essential trial documentation to ensure regulatory compliance and on-time study milestones.

You will work with cross-functional study teams, manage study documentation, and provide guidance to junior staff, contributing to process improvements and high-quality trial conduct across