Enhance your career with Oximio as a Project Specialist in clinical trial management, focusing on compliance and operational execution. Play a vital role in pharmaceutical research.Oximio is on the lookout for a Project Specialist to support its clinical trial projects effectively. This role requires 1-3 years of experience in project coordination or a related life sciences setting. You will work in close collaboration with various teams, ensuring project milestones are met while maintaining compliance with regulatory standards in a GMP environment.Key Responsibilities:Coordinate clinical trial project activities effectivelySupport packaging, labeling, and shipping operationsMaintain detailed documentation on proceduresAssist with audit preparation and compliance checksTrain junior staff in packaging processesRequirements:Bachelor's degree or equivalent educationFamiliarity with GMP and quality assurance processesStrong organizational and detail-oriented skillsProficient in MS Office toolsAbility to handle multiple tasks and prioritiesBecome an integral part of Oximio's mission to improve patient outcomes through effective clinical research processes.