London, Greater London, United Kingdom
Pharmaceuticals
Experience
Takeda Pharmaceuticals Europe Ltd April 2014 - Present
Takeda Pharmaceuticals Europe Ltd September 2013 - Present
Skills
SOP, TMF, CTMS, eTMF, Regulatory Inspection, Lifesciences, Documentation, Quality Assurance, Clinical Operations, R&D, Quality Control, PRINCE2, Training, eCRF, Regulatory Affairs, Negotiation, Phase I, Quality System, Clinical Monitoring, Pharmaceutical Industry, Change Control, Regulatory Requirements, Process Improvement, Program Management, Analysis, GxP, Oracle Clinical, Clinical Trials, EDC, Clinical Development, Project Planning, Protocol, Quality Auditing, Clinical Research, Records Management, Data Management, Document Management, CRO, GCP, Regulatory Submissions, IRB, Project Management, Regulatory Compliance, Business Process..., 21 CFR Part 11, ICH-GCP, Inspection Readiness, CAPA, SOP Development, Data Analysis