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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trial documentation and ensuring compliance with regulatory requirements, including ICH-GCP. Possesses strong organizational skills and attention to detail, facilitating effective collaboration within clinical operations teams.
Highest-signal resume keywords
Clinical Trial ManagementDocument ManagementRegulatory ComplianceOrganizational SkillsBilingual Communication
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial DocumentationQuality ControlStudy Lifecycle ManagementProcess ImprovementClinical Research Processes
Soft Skills
Attention to DetailCollaborationSupport and Guidance
Tools & Technologies
Microsoft Office
Industry Keywords
Good Clinical PracticeICH-GCPClinical ResearchSOPs
About the role
Key responsibilities & impact- Support the management and maintenance of study documentation and tracking systems
- Ensure accuracy, completeness, and quality of clinical trial records throughout the study lifecycle
- Collaborate with clinical operations teams to coordinate study-related activities and communications
- Assist with document preparation, filing, archiving, and quality control activities
- Contribute to compliance with applicable regulatory requirements, SOPs, and Good Clinical Practice (GCP)
- Provide guidance and support to junior team members when appropriate
- Participate in process improvement initiatives aimed at enhancing operational efficiency
- Support the successful execution of clinical trials
Requirements
What you’ll need- Previous experience in a Clinical Trial Assistant, Clinical Research Coordinator, Study Coordinator, or similar clinical research support role
- Minimum 2 years of experience within clinical research
- Solid organizational and document management skills
- Strong attention to detail and ability to manage multiple priorities
- Excellent communication skills in Dutch and English
- Good knowledge of Microsoft Office applications
- Understanding of ICH-GCP and clinical research processes
Benefits
Comp & perks- Flexibility to expand across sponsors and therapeutic areas
- Stability, global infrastructure, and career support of IQVIA
- Long-term IQVIA career opportunities
- Flexible work culture
- Continuous learning opportunities
- Wellbeing support