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Experienced Clinical Research Associate

About Research Drive

Research Drive B.V. is a CRO based in the northern Netherlands, with 11 employees and plans for expansion. We specialize in supporting early-phase clinical trials for pharmaceutical companies, medical tech firms, clinical research units, and other CROs. Our core value is 'Personal Business & Personal Touch.

What are you going to do?

Phase I and II Clinical Trials

As an experienced CRA or Monitor, you will be involved in Phase I and II clinical trials in the Netherlands, Belgium and Germany, taking on key responsibilities from study initiation to closure.

Client Relations and Project Management

You will be the first point of contact for our clients, working to build long-lasting relationships while managing multiple projects simultaneously.

Mentoring and Role Model

You will inspire others and act as a role model for junior CRAs following our internal training program, guiding them through their professional development.

What do we offer?

Dynamic Work Environment

You will inspire others and act as a role model for junior CRAs following our internal training program, guiding them through their professional development.

Personal Development and Growth

We value the personal development of our employees and encourage you to grow in your role, offering opportunities for further development beyond your core tasks.

Career Stability and Opportunity

We offer a contract for a minmal of 36 hours per week with the potential for a permanent position, along with the chance to assist in our internal training program for CRAs.

What do we ask of you?

Relevant Experience and Education

A completed university degree in Life Sciences or a similar field, with at least 2 years of experience as a CRA/Monitor in clinical studies.

Knowledge and Accuracy

A strong understanding of local and European laws, regulations in clinical research, and ICH-GCP guidelines, with a focus on accuracy.

Language and Communication Skills

Fluency in both Dutch and English, both spoken and written, along with a team-oriented mindset and the ability to work independently.

Your Qualities

You are accurate and thorough in your work, ensuring compliance with all regulations and guidelines in clinical research.

You enjoy working independently, taking responsibility, and proactively solving problems as they arise.

You have a collaborative mindset, working effectively with colleagues while also being able to manage your individual tasks.

Become part of our team!

If you are living in the Netherlands and identify with the profile above or would like to learn more about the role, please contact us at: .