Harrison Clinical Research GmbH

Harrison Clinical Research
Albrechtstrasse 14
80636 Munich, Germany
Tel: 49-(0)89 - 12 66 80-0
Fax 49-(0)89 - 12 66 80-2444
Homepage: www.harrisonclinical.com

Job Opportunities

Austria


Please contact us for further details, using the e-mail form below.


Position

Department

Location

Clinical Trials Administrator

Due to its continuous growth Harrison Clinical Research Eastern Europe in Vienna is looking for a Clinical Trials Administrator (CTA).
As CTA, you will be responsible for the project related preparation, collection, organisation and tracking of all study data and documentation for clinical trials phase I-IV in Denmark and abroad. This will include the setting up of systems for study conduct and handling, tracking and archiving all correspondence, study data and documentation and the preparation of study reports for sponsors, according to ICH-GCP and local regulations. You will also provide support to all functions in clinical operations and assist PMs and CRAs with their project related activities as well as cooperation and communication with HCR affiliate offices, investigational sites and the client and you will coordinate appointments, events and travel organisation.

You are preferably a life sciences graduate, or technical assistant and you have previous experience in the healthcare or life sciences area and knowledge of ICH-GCP. You have good written and spoken English and German, together with good proof reading skills, knowledge of medical terminology and MS-Office applications. You have the ability to coordinate, organise and prioritise, have an exact way of working, have good communication skills, have a good eye for detail and you are a good team player.


Clinical Operations


Vienna, Austria

Clinical Research Associate

Due to its continuous growth, Harrison Clinical Research Eastern Europe based in Vienna, Austria is looking for a Clinical Research Associate.

Duties will include investigator recruitment for national and international clinical studies and pre-study, initiation, routine and final monitoring visits to the investigational sites, coordination of all necessary regulatory documentation and the associated activities required.

The ideal candidate is a life science/medical graduate with approximately 3 years of experience as a CRA and with a good understanding of ICH-GCP.

Your ability to communicate, plan and manage your time adequately, as well as work independently to a high standard is important. Your eye for detail will be appreciated.

You are willing to travel within Czech Republic, Slovakia and Austria and occasionally to other countries.

You have excellent knowledge of written and spoken English, Czech and Slovak. It will be of advantage if you have basic knowledge in German.

You possess good knowledge of MS Office applications.
This is an exceptional opportunity to join an enthusiastic international team, pleasurable to working atmosphere and an excellent chance to be actively involved in contributing to the company’s future successes.


Clinical Operations


Vienna, Austria


  • Thank you very much for your interest in our vacancies in Austria.
  • We look forward to hearing from you.

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