Senior Project Manager, Clinical Research Operations (1-Year Contract)

What you'll be doing

• Lead and oversee Clinical Research Unit (CRU) operations to ensure efficient delivery of clinical studies, operational readiness, and alignment with organisational research priorities
• Partner internal stakeholders, sponsors, CROs, and cross-functional teams to drive successful study execution, operational planning, and issue resolution across the study lifecycle
• Provide operational leadership and subject matter expertise on clinical research processes, study feasibility, IRB submissions, regulatory requirements, and Good Clinical Practice (GCP) standards
• Support protocol reviews, study execution planning, milestone management, feasibility assessments, and operational risk mitigation initiatives
• Drive consistency and quality in study execution through process optimisation, SOP governance, CAPA implementation, root cause analysis, and continuous improvement initiatives
• Lead and oversee implementation of high-priority clinical and operational projects to support research capabilities and organisational objectives
• Ensure compliance with approved protocols, IRB requirements, regulatory frameworks, global policies, and internal SOPs across all research operations
• Participate in audits, inspections, self-assessments, and quality governance activities to maintain operational and regulatory excellence
• Oversee operational databases, research systems, equipment lifecycle management, and study-related documentation to support CRU capabilities
• Lead, mentor, and develop research operations teams while driving performance, collaboration, and workforce capability development

What we're looking for

• Bachelor Degree in Life Sciences/ Nursing/ Pharmacy/ Biomedical Sciences/ Clinical Research/ Healthcare Administration or related studies
• 10 - 12 years of working experience in clinical research operations, project management, or clinical trial management within healthcare, pharmaceutical, CRO, or research environments
• Strong knowledge of IRB processes, regulatory requirements, GCP guidelines, clinical trial operations, and research governance frameworks
• Proven experience managing cross-functional clinical study teams, operational delivery, and stakeholder engagement across complex research programmes
• Experience in audit readiness, quality management systems, CAPA processes, SOP governance, and operational compliance initiatives
• Strong analytical, problem-solving, and project management skills with ability to manage multiple high-priority studies and operational initiatives simultaneously
• Excellent communication, leadership, and stakeholder management skills with confidence engaging sponsors, investigators, CROs, and senior leadership
• Experience leading teams and driving operational transformation or process improvement initiatives will be highly advantageous

Interested applicants, kindly furnish us with your full and detailed resume in MS Words format and click "Apply Now" button.

We regret to inform only shortlisted candidates will be notified. Applicants who do not possess necessary experience or qualification will still be considered on individual merits and may be contacted for other opportunities. 

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