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Senior CTA

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01 DEC ’21: For an organisation offering an innovative combination of drug development knowledge, clinical trial design, and management, we are looking for a Clinical Trial Assistant. Currently, they have operations throughout Europe, in countries such as France, Germany and Ireland and facilities in the UK and US. Their mission is to play a vital role in the development of new products that allow disease prevention and treatment. They do this by creating an environment where you as a professional can develop yourself and apply your valued talents. This organisation nurtures a place where respect, pro activity, teamwork and patience are core values. Due to the growth of the company, they are now looking for a Clinical Trial Assistant, who is excited to be the steady support unit of the Clinical Project Manager. The team consists of six people, among them are medical writers and project managers.

  • Clinical Research
  • Clinical Research
  • Breda
  • 40 hours p/week
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About your role

This is how you will make the difference

As a Clinical Trial Assistant, you will be involved in the entire proces from initiation, planning, execution, controlling and closing of the clinical trials. As you will not be having the end-responsibility of the projects, you will function as a support unit to all aspects of Clinical Project Management. This means that this is a unique opportunity to learn everything about project management hands-on and catapult your career within Clinical Research. There is much to discover because of the ranges of services that are being offered, you can grow in multiple areas: Regulatory Affairs, Business Development and for example Account Management. What is important from the start is that you understand the baseline of Clinical Trials, the different stakeholders and the dynamic between sponsors, sites, monitors and external vendors. This in combination with the administrative knowledge of all relevant documents and protocols will open up the door to you to become a Clinical Trial Assistant.

What's needed

What you bring

What are we looking for in the ideal candidate:

  • BSc or MSc in a relevant discipline
  • Two years experience working in clinical trials, specifically phase I
  • ETMF (Electronic Trial Master File) experience
  • EMA/FDA and GCP knowledge
  • Experience in early drug development
  • An assertive and pro-active attitude
  • Analytical mindset
  • A good team player who is able to form positive relationships

What we offer

What's in it for you

In return for your time and energy we offer:

  • A great opportunity to learn everything about Clinical Project Management
  • Different studies within a wide range of therapeutic area’s and clients
  • A base salary with a midpoint of around €44,500.- gross per year
  • Great secondary benefits like a fully covered pension plan
  • Very nice internal culture with kind and able minded people
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