Clinical Research Associate (CRA) – Oncology
Germany
Full Time
3 weeks ago
Visa Sponsorship
Key skills
Google Cloud PlatformGCPGoogle CloudAgile
About this role
Role Overview
- Monitoring clinical trials across various oncology therapeutic areas
- Ensuring the accurate, complete, and timely transmission of study data
- Timely preparation of high-quality reports and follow-up letters for monitoring visits
- Participation in international study team meetings and investigator meetings
- Initiation of study sites, training, support and guidance for site staff
Requirements
- University degree in a scientific or medical discipline or equivalent
- At least two years of relevant experience as a monitor in the conduct of clinical trials
- Solid knowledge of ICH-GCP and a confident handling of legal and regulatory requirements
- Experience using electronic Case Report Forms (eCRFs) and preparing monitoring reports
- Excellent English skills
Tech Stack
- Google Cloud Platform
Benefits
- Individual development opportunities with a focus on lifelong learning
- A high level of trust, appreciation and opportunities to contribute within a focused and passionate team
- Office space in the heart of Hamburg that enables collaborative, flexible and agile working
- A diverse, inclusive and bias-free working environment
- A sustainable company committed to becoming carbon-negative across the entire value chain by 2030