CRA - Clinical Research Associate - Clinical Research

Paramount Recruitment currently have several vacancies for Clinical Research Associates CRA’s II III throughout Europe with the top CRO’s Clinical Research Organisation’s and Pharmaceutical companies. There are positions available across a range of therapeutic areas.

As a CRA Clinical Research Associate you will be working on phase I - IV studies and will be responsible for:

* Adhering to SOP’s, ICH-GCP and other local regulations.
* Contributing to documentation design, to include Case Report Forms.
* Performing initiation visits.
* Performing monitoring visits.
* Planning and organising study-related meetings.
* Managing the reporting of adverse events.
* Collecting high quality data.

Ideal candidates will have a clinical or science related degree as well as at least 1 year’s experience as a CRA Clinical Research Associate within a Clinical Research Organisation or Pharmaceutical company. Strong communication skills are also required. Fluency in both the local language and English are essential.

For more information on these roles or any other clinical vacancies please call Marie Tucker on +44 121 616 3470.

Keywords: CRA, Clinical Research Associate, CRO, Clinical Research Organisation, Pharmaceutical, Europe, Germany, Croatia, Russia, Hungary, Portugal, Spain, France, Italy, Netherlands

Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.