Leyden Labs
51 - 200 employees
💰 $140M Series B on 2022-01
Leyden Labs aims to help people live their lives to the fullest. Our platform targets commonalities of viral families to protect humanity from known and future viruses. Our portfolio of accessible intranasal product candidates may provide people with the freedom to immediately protect themselves from and prevent the spread of many variants of respiratory viruses, including ones in the influenza and coronavirus families.
Senior Clinical Trial Associate
🔥 0 minutes ago
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
Leyden Labs
51 - 200 employees
💰 $140M Series B on 2022-01
Leyden Labs aims to help people live their lives to the fullest. Our platform targets commonalities of viral families to protect humanity from known and future viruses. Our portfolio of accessible intranasal product candidates may provide people with the freedom to immediately protect themselves from and prevent the spread of many variants of respiratory viruses, including ones in the influenza and coronavirus families.
📋 Description
• Assist the Clinical Trial Teams in ensuring the most effective and efficient conduct of clinical trials by providing administrative and project tracking support • Support the preparation, handling, distribution, collection and archiving of clinical study documents and reports, including contracts and invoices • Ensure that all study files are periodically reviewed for completeness and maintained in accordance with Good Clinical Practices, applicable regulations and company procedures • Interface with internal colleagues and external vendors and partners • Work closely with the Clinical Operations Team to support the effective execution of clinical studies and maintain high standards of quality and compliance
🎯 Requirements
• Master's degree in a life science related field • At least 5 years’ experience in a CTA role in a bio-pharmaceutical and/or CRO environment • Proven training in/knowledge of GCP and International Conference on Harmonization (ICH) Guidelines • Previous experience working with eTMF, EDC, IRT/RTSM, CTMS systems • Ability to independently manage documentation and team support needs • Computer skills including working knowledge of Microsoft Word, Excel, PowerPoint, and SharePoint • Excellent verbal and written communication skills in English • Currently residing in the Netherlands with EU work authorization • Available for 32-40 hours per week until December 2026.
🏖️ Benefits
• Occasional travel to the Leiden office could be requested 1-2 times per month.
Apply Now
