Senior Clinical Trial Assistant - Sponsor dedicated - Netherlands- Hybrid (m/w/d)
Core
Support the management and maintenance of study documentation and tracking systems for clinical trials across all phases of development.
Role type
Senior Clinical Trial Assistant (Sponsor dedicated)
Builds
Clinical trial documentation and processes for pharmaceutical and biotechnology sponsors
Domain
Clinical research / Life sciences
Required skills
Study documentation management, Regulatory compliance (GCP), Document preparation and archiving, Process improvement, Team collaboration, Multi-priority management
Preferred skills
ICH-GCP knowledge, Microsoft Office proficiency
Technologies
Microsoft Office
Responsibilities
Support management and maintenance of study documentation and tracking systems; Ensure accuracy, completeness, and quality of clinical trial records; Collaborate with clinical operations teams to coordinate study-related activities; Assist with document preparation, filing, archiving, and quality control; Contribute to compliance with applicable regulatory requirements, SOPs, and Good Clinical Practice (GCP); Provide guidance and support to junior team members; Participate in process improvement initiatives.
Seniority
Senior, hands-on IC
