Job description

[This job id 7581 first appeared in Job-Q.com on 17 May 2026]

📍 Location: Buona Vista
🕒 Mon–Fri, 8.30am–5.30pm
💰 Up to $14,000/month (based on experience)
📄 Contract role

🔬 Key Responsibilities

• Lead operational planning and execution of clinical studies
• Coordinate between CRU and sponsor cross-functional teams
• Ensure adherence to study protocols, timelines, and regulatory requirements
• Support IRB/regulatory submissions and operational alignment
• Drive communication, issue resolution, and study performance tracking
• Maintain study documentation, metrics, and operational databases
• Lead post-study reviews and process improvements
• Supervise and guide CRU team members

🎯 Requirements

• Degree in Science / Health / Life Sciences or related field
• Minimum 5 years clinical research experience (PM/operations)
• Experience in early-phase clinical trials preferred
• Strong leadership, communication, and stakeholder management skills
• Good understanding of clinical trial processes and regulations
• Ability to manage cross-functional and global teams

To apply, please click on “Apply Now” or email your latest resume to dorothy@recruitlync.com / WhatsApp 85017683.

Ooi Shi Hui Dorothy (R1762852)

Recruit Lync Pte Ltd (22C1000)

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