Clinical Project Manager

TRITON AI PTE. LTD.; Singapore; On-site; SGD 80,000 - 120,000; Full time

Job summary

A leading healthcare organization in Singapore is seeking a Clinical Operations Manager to lead pivotal vaccine trials in Southeast Asia. The candidate will manage project strategies, ensure compliance with regulations, and engage stakeholders throughout the trial phases. Extensive experience in clinical operations and project management is required, particularly in vaccine studies. This role offers the opportunity to impact public health through innovative research.

Qualifications

• 5+ years in clinical operations with project management experience.
• Demonstrated clinical trial experience, especially in vaccines.
• Familiarity with Southeast Asian regulatory landscapes.

Responsibilities

• Manage operational strategy, timelines, budgets for vaccine trials.
• Oversee site selection, initiation, monitoring, and compliance.
• Lead CROs and vendors to deliver quality data.

Skills

Clinical operations management

Project management

Regulatory compliance

Stakeholder engagement

Risk management

Education

Bachelor's degree in Life Sciences

Advanced degree (preferred)

Job description

The Opportunity

Lead pivotal vaccine trials across diverse Southeast Asian markets. You'll ensure regional study delivery from initiation to close-out, collaborating with cross-functional teams to advance the portfolio in infectious diseases.

Key Responsibilities

• End-to-End Project Leadership: Manage regional operational strategy, timelines, budgets, and risk mitigation for Phase II-IV vaccine trials across SEA (Singapore, Malaysia, Thailand, Indonesia, Vietnam, Philippines)
• Site Excellence: Oversee site selection, initiation, monitoring, and close-out activities, ensuring compliance with ICH-GCP and local regulations
• Vendor Partnership: Lead CROs, central labs, and regional vendors to deliver quality data on schedule
• Stakeholder Engagement: Serve as primary point of contact for investigators, internal teams (Medical, Regulatory, Data Management), and country managers
• Risk Management: Proactively identify and resolve operational challenges across diverse regulatory environments
• Resource Stewardship: Manage regional budgets and mentor junior CRAs

Required Qualifications

• Experience: 5+ years in clinical operations with 2+ years’ direct project management experience leading multi-country multi-site trials
• Therapeutic Expertise: Demonstrated clinical trial experience Phase I-III, experience in vaccines trials
• Regional Knowledge: Proven success managing studies in Southeast Asia; familiarity with country-specific regulatory landscapes
• Technical Skills: Mastery of ICH-GCP, clinical trial management systems (CTMS), and risk-based monitoring
• Education: Bachelor’s degree in Life Sciences (Advanced degree preferred)

Interested applicants please include a summary table about your different clinical trial projects, including the TA, indication & Phase, your role & involvement, country coverage, study sample / size.

License no. 21C0661

Reg No. R1331018