As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.
You will build and maintain relationships with clinical sites and investigators.
Your focus will be on subjects’ rights, safety and well-being and quality of data compliance.
Responsibilities will include conducting and reporting all types of onsite monitoring visits, driving the study startup phase, performing CRF reviews, source document verification and query resolution.

BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
Independent on-site monitoring experience in the Netherlands
Demonstrable experience in all types of monitoring visits in Phase II and/or III
Strong written and verbal communication skills
Fluency in Dutch and English
Experience supporting Oncology studies is beneficial, but not essential
Advanced knowledge of MS Office
Full and clean driver's license, and the ability to travel
Communication, collaboration, and problem-solving skills are essential
Ability to multitask and work in a dynamic team environment

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Senior Clinical Research Associate

Key skills