Are you a talented Clinical Trial Assistant with a passion for clinical research? We're looking for an experienced Freelance CTA to join a dynamic team supporting cutting-edge studies
Non si lasci sfuggire questa opportunità: si candidi rapidamente se la sua esperienza e le sue competenze corrispondono a quanto descritto di seguito.
Key Responsibilities:
* Assist in the management and oversight of clinical trials across various therapeutic areas, including ophthalmology, neurology, and rare diseases.
* Support Clinical Research Associates (CRAs) and Regulatory and Start-Up Specialists (RSU) with study documentation, site compliance, and study performance tracking.
* Prepare, distribute, and archive clinical trial documentation in line with standard operating procedures.
* Assist in the preparation and maintenance of clinical trial supplies, site communications, and regulatory submissions.
* Review study files for completeness and accuracy, ensuring compliance with study protocols and good clinical practice (GCP).
What We're Looking For:
* 5+ years of experience as a Clinical Trial Assistant (CTA) or similar role within CRO or pharmaceutical environments.
* Hands-on experience supporting global clinical project teams and understanding of clinical trial operations.
* Strong knowledge of clinical trial systems like eTMF and Veeva Vault (or similar).
* A background in ophthalmology, neurology, or rare disease studies is preferred but not essential.
* Ability to work full-time on a 12-month contract.
* Must be able to work onsite in Milan at least 3 days per week. xrdztoy
* Fluency in English (B2 level or higher), with strong written and verbal communication skills.