Clinical Project Specialist

Monday - Friday Completion Bonus Buona Vista Join a leading global pharmaceutical company as a Clinical Project Specialist, responsible for the effective management and implementation of clinical trials within the Clinical Research Unit (CRU), ensuring compliance with GCP, SOPs and regulatory requirements. Key Responsibilities Manage clinical studies from planning and implementation through to close-out. Act as the primary liaison between the CRU, Sponsors, investigators, monitors, vendors and Ethics/Institutional Review Boards. Coordinate study timelines, site initiation, monitoring and close-out visits, training and study meetings. Support protocol and study document development, regulatory submissions, safety reporting and trial documentation. Monitor study progress, risks, issues and deliverables, and coordinate timely resolution with relevant stakeholders. Manage study-related vendors, supplies and budget tracking. Support audits, inspections, SOP updates and process improvement initiatives. Requirements: Minimum Degree in Nursing, Sciences, Health related or Management field Minimum 5 years of Clinical Research Coordination Experience Willing to travel overseas We regret to inform you that only shortlisted candidates will be notified.

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