Sr Clinical Trial Assistant

Job Duties:Set up, maintain, and reconcile the electronic Trial Master File (eTMF) while supporting audit and inspection readiness.Develop and maintain study management trackers, spreadsheets, and filing systems across multiple programs.Track purchase orders, vendor invoices, study agreements, and contract routing.Coordinate biological sample shipments to central and reference laboratories.Manage site feasibility data, route document approval forms, request liability insurance, and support ClinicalTrials.gov registry activities.Assist in planning internal and external study meetings, including managing agendas and minutes.Provide required documentation (such as FDA Form 1572) to Regulatory Affairs for submissions.QualificationsBachelor's in life sciences or a related fieldAt least 3 years of relevant industry experienceOncology experience (Phase I-III)Global trialsClinical software (eTMF, CTMS, etc.)**Remote****Long-Term Contract****No 3rd parties*