Why clinical trials?

Because medical progress concerns us all.

Nobody wants to fall ill. And those who are ill want effective, safe and well-tested treatment options.

That is exactly why clinical trials are necessary: they show whether new medicines, medical devices or treatment methods really help, can be applied safely and bring measurable benefit to patients.

Clinical research is therefore not just a regulatory step on the way to approval. It is a shared contribution to better medicine — for today's patients and for those who will depend on new therapies tomorrow.

For trials to be conducted reliably, clear structures, trained teams and consistent quality assurance are needed.

Quality in daily trial operations

What makes clinical trials successful.

A.

Patient safety

Participants must be protected, supported and cared for according to clear requirements.

B.

Plannable delivery

Trial visits, workflows, materials and responsibilities must be precisely coordinated.

C.

Reliable documentation

Data must be captured completely, traceably and in a quality-assured way.

D.

Clear communication

Clinical trials only work when everyone involved is well aligned — from medical responsibility through the study nurse to the participant.

E.

Scientific value

Only robust trial data enables approval, publication and medical progress.

What do study nurses & study coordinators do?

The key role in daily trial operations.

Study nurses and study coordinators are often the central link between participants, investigators, trial team, sponsor and CRO. They make sure clinical trials work in everyday practice — organised, understandable, patient-centred and quality-assured.

They accompany participants, coordinate workflows, keep track of appointments and requirements, and ensure that trial-related activities are documented traceably. In doing so, they contribute substantially to trials being not just planned, but reliably delivered.

Typical tasks in daily trial operations

This role requires precision, a sense of responsibility, strong communication skills and a good understanding of people as well as trial processes. Study nurses and study coordinators are thus a decisive factor for quality, continuity and trust in clinical trials.

Application

Become part of the VALEA network.

VALEA Clinical works project-based with qualified study nurses and study coordinators across Austria — and also supports those entering clinical trial practice.

After your application, we will get in touch for a non-binding initial conversation. You can send us your CV and qualification documents directly afterwards.

  • 01Submit your application
  • 02Non-binding initial conversation with Valentina Jovanoska
  • 03Project-based collaboration — matched to your region and availability

Apply now

We will get back to you within a few working days.

Your first conversation with VALEA — free and non-binding.

Valentina Jovanoska will gladly walk you through the necessary qualifications and the tailored support we offer for your path in clinical research.