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

Ukraine


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


Position

Department

Location

Clinical Research Associate (CRA)

Due to its continuous growth Harrison Clinical Research Ukraine is looking for an experienced 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 this requires.

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

Your ability to communicate, plan and manage your time adequately, work  with  the international team as well as independently to a high standard is essential and you have a good eye for detail.

You are willing to travel within the Ukraine and occasionally to other countries.

You have excellent knowledge of written and spoken English, Ukrainian and native Russian languages and you possess good knowledge of MS Office applications.


Clinical Operations


Kiev, Ukraine

Senior Clinical Research Associate (SCRA)

Due to its continuous growth Harrison Clinical Research Ukraine is looking for a Senior Clinical Research Associate who will take on the lead CRA function.
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 this requires. As a lead CRA, additional duties include project coordinating and mentoring of the junior CRAs.

The ideal candidate is a life science/medical graduate with at least 3 years of experience as a CRA and with a good understanding of ICH-GCP and local clinical trial legislation.
Your ability to communicate, plan and manage your time adequately, as well as work independently to a high standard is important and you have a good eye for detail.
You are willing to travel within Ukraine and occasionally to other countries.

You have excellent knowledge of written and spoken English, Ukrainian and native Russian and you have experience working on projects conducted for US client(s) and experience in the preparation/participation of clinical trial inspections would be an advantage. You possess good knowledge of MS Office applications.


Clinical Operations


Kiev, Ukraine


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

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