Beschreibung
Responsibilities:- Management of all documents and logistical and administrative tasks related to trial start-up, execution and close out of clinical trials
- Performance of technical regulatory document review
- ensures trial related activities are in compliance with SOPs, policies and local regulatory requirements
- operational oversight from start-up through to database lock and closeout
Requirements:
- Minimum of 3 years of related work experience as a Clinical Trial Assistant (CTA)
- Demonstrated ability to work in a position demanding strong communication skills
- Must be well organized and adaptable
- Experience with multiple software systems as well as other tracking / CTMS, eTMF/LAF, Trial Master Source, Sharepoints
- English / German: fluent
Startdate: ASAP
Duration: 6 Months
Volume: 100% (40 h / Woche)
Location: on site, NRW, Germany
If you are interested, feel free to contact me right away. I will get back to you as soon as possible.