. Requirements: Bachelor's degree in clinical, biological, or mathematical sciences, nursing, or a related field. Minimum of 6...
in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
Responsibilities: Involve in Supplier Issue Resolution. Work on Corrective Actions Implementation, Collaborate w/ cross functional team during issue resolution, Develop & Propose supplier Improvement Plan. Proliferate Key learnings & Do...
Roles and Responsibilities: Strong writing, grammar, and editing abilities to create clear and concise documentation. Ability to adapt writing style to various audiences (e.g., end users, technical teams, or regulatory bodies). Docume...
Responsibilities: Author, review, and execute validation protocols (IQ, OQ, TMV, PQ) for process validation and re-validation activities in compliance with FDA/AAMI/ISO/EN guidelines/standards. Actively participate in all phases of proce...