Castor
Biotechnology • Pharmaceuticals • Healthcare Insurance
Castor is a modern clinical trials platform designed to facilitate research data management and patient experiences in clinical studies. It offers solutions such as Electronic Data Capture (EDC), electronic Patient Reported Outcomes (ePRO), and electronic Consent (eConsent), ensuring secure and compliant processes in line with industry standards like GDPR and HIPAA. The platform supports decentralized clinical trials (DCT) and integrates various sources to manage real-world evidence efficiently. Castor positions itself as user-friendly and supports academic, biotech, and pharmaceutical research sectors.
Senior Data Manager
November 8
Castor
Biotechnology • Pharmaceuticals • Healthcare Insurance
Castor is a modern clinical trials platform designed to facilitate research data management and patient experiences in clinical studies. It offers solutions such as Electronic Data Capture (EDC), electronic Patient Reported Outcomes (ePRO), and electronic Consent (eConsent), ensuring secure and compliant processes in line with industry standards like GDPR and HIPAA. The platform supports decentralized clinical trials (DCT) and integrates various sources to manage real-world evidence efficiently. Castor positions itself as user-friendly and supports academic, biotech, and pharmaceutical research sectors.
📋 Description
• Accountable leader for the quality and integrity of data across complex clinical programs. • Responsible for driving standards, ensuring regulatory compliance (GCP/ICH). • Leading the Data Management lifecycle from database setup to final database lock and submission for clinical trials/programs. • Ensuring the robustness of data that fuels life-changing medical research.
🎯 Requirements
• Minimum of 5-8+ years in Clinical Data Management, with significant tenure working on complex, global studies • Expert-level proficiency with leading EDC systems and advanced understanding of data standards • Deep, applied knowledge of ICH-GCP, 21 CFR Part 11, and experience contributing to regulatory submission packages. • Demonstrated experience formally or informally mentoring others on complex processes and quality best practices.
🏖️ Benefits
• Guaranteed annual ‘happy holidays’ bonus • Employee Stock Option Plan • Learning & Development Budget to support your growth • Unlimited annual leave (25 days minimum) • A fully remote role, with support for your home office set-up • A flexible working schedule: nobody is tracking your time except you, we focus on output and delivery • A great work-life balance • Quarterly downtime weeks, well-being workshops, sleeping courses (for you and for new-borns) • access to OpenUp, virtual company events and celebrations
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