CareerPlan

Studienassistenz (m/w/d) in der Studienzentrale

Leverkusen, NORDRHEIN_WESTFALENFull-time2026-07-23 → 2026-11-11

Core

Support the preparation of clinical study concepts and applications, coordinate study visits and patient recruitment, and manage study data documentation and medication storage.

Role type

Clinical Trial Assistant (Study Support)

Builds

Clinical study operations and data management for pharmaceutical trials

Domain

Healthcare / Clinical Research / Oncology

Required skills

Clinical trial preparation, Study concept development, Regulatory compliance, Data documentation, Patient registration, Medication management, Query resolution, Audit preparation

Preferred skills

GCP certification, Oncology knowledge, Practical clinical trial experience, PC proficiency

Responsibilities

Prepare clinical study concepts and applications, Coordinate study visits and patient recruitment, Document study data in German and English, Manage storage and inventory of trial medication, Handle sponsor queries and adverse event reporting, Prepare for audits and inspections, Archive study documents