Our client is a Clinical Research Organisation (CRO) focused on delivering highquality clinical operations and project management services across AsiaPacific and global markets. They are seeking an experienced Clinical Project Manager to lead and oversee the end-to-end clinical trial operations and serve as the primary liaison between internal teams, clinical sites, and sponsors. You will drive timelines, manage budgets, safeguard compliance, and ensure successful study delivery.
Responsibilities:
- Lead and manage the full lifecycle of clinical trials from startup to closeout, ensuring delivery on time and within budget.
- Serve as the primary point of contact for sponsors, clinical sites, and internal crossfunctional teams.
- Oversee site feasibility, selection, initiation, monitoring activities, and overall study conduct in compliance with ICHGCP and regulatory requirements.
- Track study progress, timelines, risks, and performance metrics, implementing mitigation strategies when needed.
- Coordinate and manage external vendors, laboratories, and service providers to ensure quality and timely deliverables.
- Prepare and lead study meetings, including kickoff meetings, investigator meetings, and regular sponsor updates.
- Maintain accurate study documentation, ensure audit readiness, and support quality assurance activities throughout the study.
Requirements:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related discipline (Master's preferred).
- At least 2 years of clinical project management experience within CRO, biotech, or pharma.
- Strong knowledge of ICHGCP, clinical trial regulations, and operational processes.
- Demonstrated ability to lead crossfunctional teams and manage multiple priorities.
- Excellent communication, stakeholder management, and problemsolving skills.
If you are interested, please apply with your CV attached.
