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. Recruit Lync | 22C1000 Choek Wei Qi Joel | R1877109