Clinical Study Administrator / Clinical Trials Assistant (w/m/d) – Zelltherapie
Core
Coordinate and administer clinical trials across all phases, serving as the central contact for clinical sites and ensuring timely delivery of study results.
Role type
Clinical Study Administrator (CSA)
Builds
Interventional clinical studies for cell therapy
Domain
Life Sciences / Cell Therapy / Clinical Operations
Deliverable
client delivery
Required skills
ICH-GCP knowledge, document management, regulatory compliance, study tracking tools, contract preparation, meeting organization, translation coordination
Preferred skills
Prior experience in clinical trials or clinical operations, familiarity with study management systems
Technologies
eTMF, ISF, CTMS, MS Office
Responsibilities
Coordinate study administration from initiation to close-out; manage regulatory and study documents; ensure proper maintenance of eTMF and ISF; update study information in tracking tools; prepare site contracts and coordinate study materials; organize study meetings and support audits; archive study documentation.
Seniority
Entry-level to Mid-level, hands-on IC
