Clinical Research Operations Manager (CRU)

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)