Location:
Wilmington, North Carolina Area
Skills:
Adobe Acrobat, Word, Excel, FDA, Clinical, Microsoft Excel, Clinical Research, Microsoft Word, GCP, Project Management, Data Entry, GMP, Validation, Microsoft Office, Program Management, Visio, Management, Oncology, Biotechnology, Healthcare, Regulatory Submissions, Process Scheduler, Fundraising, LIMS, Data Analysis, Research, EDC, Medical Writing, Quality Assurance, Process Improvement, Sop, Quality Control, Training, Clinical Data Management, Regulatory Requirements, Software Documentation, GLP, Biostatistics, Data Management, Regulatory Affairs, CRO, Outlook, Pharmaceutical Industry, Public Speaking, Clinical Development, Strategic Planning, PowerPoint, Lifesciences, ICH-GCP, 21 CFR Part 11