Leyden Labs
Biotech
FreelanceSr.ClinicalTrialAssociate
“Freelance Sr. Clinical Trial Associate at Leyden Labs. Skills: Clinical trial support, ETMF maintenance, GCP compliance. Assist Clinical Trial Teams. Provide administrative support”
Industry & Context.
What They're Looking For.
Must Have
Master's degree, 5+ years CTA experience, GCP knowledge, ICH Guidelines knowledge, ETMF experience, EDC experience, IRT/RTSM experience, CTMS systems experience, Independently manage documentation, Computer skills, Microsoft Word proficiency, Microsoft Excel proficiency, Microsoft PowerPoint proficiency, SharePoint proficiency
Nice to Have
Residing in the Netherlands
What You'll Do.
Assist Clinical Trial Teams
Provide administrative support
Provide project tracking support
Support preparation of documents
Support handling of documents
Support distribution of documents
Support collection of documents
Support archiving of documents
Ensure study files reviewed
Interface with internal colleagues
Interface with external vendors
Interface with partners
Support effective execution of studies
Maintain high standards of quality
Maintain high standards of compliance
How You'll Work.
Team & Collaboration
Clinical Operations Team; Internal colleagues; External vendors; External partners
Communication Scope
Verbal communication; Written communication
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