Clinical Project Manager
Our client is a Clinical Research Organisation (CRO) focused on delivering high‑quality clinical operations and project management services across Asia‑Pacific 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 start‑up to close‑out, ensuring delivery on time and within budget.
- Serve as the primary point of contact for sponsors, clinical sites, and internal cross‑functional teams.
- Oversee site feasibility, selection, initiation, monitoring activities, and overall study conduct in compliance with ICH‑GCP 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 kick‑off 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 ICH‑GCP, clinical trial regulations, and operational processes.
- Demonstrated ability to lead cross‑functional teams and manage multiple priorities.
- Excellent communication, stakeholder management, and problem‑solving skills.
If you are interested, please apply with your CV attached.
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