About this role

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices
Develop and implement tools, procedures, and processes to ensure quality monitoring
Contribute to the design, implementation, and delivery of processes, programs, and policies
Manage defined components of projects or processes within the area of responsibility
Ensure accurate and timely documentation of monitoring activities and findings
Collaborate with cross-functional teams to support clinical trial operations

Bachelor's degree in a related field or equivalent experience
Minimum of 2-4 years of experience in clinical research monitoring
Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
Excellent communication and interpersonal skills
Fluency in Dutch
Ability to work independently and manage multiple priorities
Proficiency in using clinical trial management systems and other relevant software

We are passionate about developing our people, through career development and progression
supportive and engaged line management
technical and therapeutic area training
peer recognition and total rewards program
We are committed to building an inclusive culture – where you can authentically be yourself.

Clinical Research Associate II – Sponsor Dedicated

Key skills