Clinical Research Associate II and Senior Clinical Research Associate

Are you a CRA looking for the best of both worlds? Would you like to work directly with a single sponsor while still enjoying the stability, global reach, and career development opportunities that come with working for a leading CRO? Our team calls it the best of both worlds — and we think you’ll agree.

ClinChoice is a rapidly growing global contract research organization. We’re currently expanding our CRA network in the Netherlands and looking for talented Clinical Research Associates (CRA II and Senior CRA) interested in partnering with some of the world’s leading pharmaceutical companies in the field of biomedicine. If that sounds like you, we encourage you to submit your resume via our website — we’d love to hear from you!

Position Overview – Clinical Research Associate As a CRA, you’ll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices. You will oversee site performance, conduct company-initiated clinical studies, and ensure high-quality deliverables through site visits, monitoring, and effective communication.

Requirements

: Willingness to travel to sites and surrounding countries (50-80% travel). Fluent in Dutch (required for work in the Netherlands). Prior experience in monitoring clinical trials and site management.

Join a dynamic, global team that values growth, collaboration, and making a difference in clinical research.

of the role. Up to 8 years of experience as a CRA.

Sound knowledge of medical terminology. Fluent in English and local language(s). g.

Word, Excel, Outlook). Education and Experience: A Bachelor Degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science, a Masters or PhD/MD/PharmD. At least 4 plus years of onsite monitoring experience is required.

Previous medical device monitoring experience is required. Therapeutic area experience in neuro- or cardiovascular domain is also required. Requires understanding and application of regulations and standards applied in clinical research areas and medical devices/combination products.

, CCRA, RAC, CDE). Clinical/medical background – a plus. Languages: Be able to converse and monitor in English and Dutch.

Must be able to converse and understand the documentation, monitoring, etc. in a reasonably confident manner to monitor in that. Ability to travel up to 80% of time.

The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it.

we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for?

About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

Qualifications

: Bachelor's Degree or equivalent University Degree in scientific and/or medical or paramedical disciplines; Nursing degree or relevant degree or background preferred.