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Posted yesterday by Taylorollinson
Prior experience as a Regulatory Specialist within IVD or Medical Devices. Excellent understanding of ISO13485, ISO17025 and cGMP. Familiarity in regulatory submission processes within Medical Devices or diagnostics. Familiarity with EMEA and LATAM regions is beneficial. Experience … more
Posted just now by CK Group- Science, Clinical and Technical
Be responsible for writing Statistical Analysis Plans (SAPs), developing medical code lists for studies, guiding data analysts to explore large healthcare databases and interpreting the study results and outputs. Contributes to projects using real-world healthcare data assets and guide … more
