Beschreibung
Currently I am looking for a Freelance Clinical Trial Assistant to support one of our clients.The client is a well-known and international company based in Hessen, Germany.
Responsibilities:
- Trial Master File maintenance and filing of relevant documents according to ICH-GCP and SOPs (as required), respective archiving and electronic filing of documents.
- Assistance with the preparation/collection of all study documents (e.g. protocol, CRF, forms, manuals, contracts, etc.) and presentation materials.
- Support with study start up activities (e.g. review of study specific documents provided by CRO, participation in User Acceptance Testing, etc.).
- Support with tracking timelines/deliverables
- Track various program-related activities/documents such as project team calendars, monitoring frequency and others. Periodically distribute tracking documents to predetermined contacts.
Requirements:
- Minimum of two 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 / spreadsheet software systems
- English (very good), German (optional)
Startdate:
Duration: 12 Months
Volume: 100% (40 h / Woche)
Location: on site, Hessen, Germany
If you are interested, feel free to contact me right away!