This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Specializing in oncology, Kapadi excels at navigating the early stages of drug development, providing comprehensive and custom curated CRO solutions to biotech companies ready to move their immuno-oncology assets from concept to clinic. Kapadi is part of the NEUCA Group. We are the industry leading global oncology CRO supporting biotech partners to accelerate innovative research.
Job Responsibility:
site and project coordination: act as the main point of contact for clinical sites throughout the study lifecycle, providing support for site initiation, compliance, and regulatory documentation
documentation & tracking: maintain and update project documentation, tracking activities, site status, and action items according to SOPs
regulatory maintenance: oversee regulatory updates, including protocol amendments, safety reports, and IRB/IEC submissions, ensuring all documentation is current and compliant
training & compliance: complete required training and keep up-to-date with ICH-GCP guidelines and relevant local regulations
budget and contract: oversight and liaison between site and sponsor with budget and contracts
Requirements:
proven 5+ years of experience in study start-up processes in clinical research
a medical-related university degree
working knowledge of ICH-GCP and local regulatory guidelines
strong communication, organizational, and multitasking skills
What we offer:
remote work opportunities
professional development in a well‑established company with a strong market position
employment in a company awarded the Top Employer 2026 certificate – we create a work environment based on trust, collaboration, and diversity
a comprehensive benefits package in the form of a cafeteria system – you decide which benefits best suit your needs