The posting
- 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



