Description
Are you an expert in Clinical Monitoring? Then you are the right man for this job!We are searching a (Senior) CRA for our client in Germany doing monitoring work in Poland. You should bring along the following skills:
- Study of life sciences or a related field of study
- 3 or more years practical experience
- Good ICH-GCP knowledge
- Teamplayer, hands-on-worker
- Fluency in Polish and advanced English language skills
- Willingness to travel
Project description:
- monitoring of clinical trials and side visits in Poland
- Interface with the sponsor local study team to ensure timely initiation and completion of clinical trials
- Data collection and preparation and review of regulatory documents
- Process Management according to ICH-GCP standards, local requirements and SOPs
- Start-up, maintenance and closure of clinical studies
Startdate: Asap (February or March)
Volume: full-time
Location: office or homebased (monitoring the sides in Poland)
Freelance or temporary work
Are you interested in this Project?
If you are not interested in this project please feel free to forward this email to your colleagues or friends.
Looking forward to hear or read from you,
Kind regards,
Stefan