South Clinical Trial Operations Manager
Location : Singapore | Posted : Nov 24, 2025
Working Hours :
- 8am – 5pm / 9am – 6pm
- Fully on site
Summary
The Senior Manager, Operations will head a team responsible for producing clinical trial supplies, including pre‑production and planning, label production and manufacturing and packaging.Provide leadership and direction to deliver on business strategy, meet client requirements, achieve regulatory standards, ensure on‑time delivery, quality, and efficiency targets, and establish safe working practices within a GMP environment.Key member of the Site Leadership Team.Selected Responsibilities
Leadership and Management : Provide direct leadership to the production team.Resource Allocation : Use S&OP data and production plans to manage staffing and risk mitigation.Risk Mitigation : Resolve workflow or technical issues that could disrupt operations.Technical Review : Oversee timely technical review of batch records.Stakeholder Partnership : Maintain close partnerships with PM, QA, Supply Chain.Operational Performance Management : Manage KPIs, participate in target setting, and report monthly.Continuous Improvement : Implement strategies to reduce costs, waste and increase output.Regulatory Compliance : Maintain audit‑ready state and adhere to facility EHS regulations.Audit Support : Represent operations during QA, client audits and provide responses and CAPAs.Quality Incident Management : Investigate quality incidents and implement CAPAs.Metrics & Reporting : Track and report metrics to senior management.Financial & Non‑Financial Objectives : Support site head with financial planning and operating budgets.System Knowledge : Basic working knowledge of Clinicopia, JDE, SupplyFlex and related platforms.Line Management Responsibilities
Training and Compliance : Ensure team members follow SOPs.Staffing and Development : Conduct regular one‑on‑one meetings and support career development.Team Development : Hold operational team meetings to foster collaboration.Goal Implementation : Align departmental goals with company objectives.Coaching and Mentoring : Provide ongoing coaching for direct reports.Employee Relations : Manage performance evaluations, hiring, disciplinary actions, and recognitions.Administrative Approvals : Approve holiday requests and expenses.Requirements
Minimum degree.Experience in pharmaceutical / biotech / clinical research organization.Strong leadership skills; ability to oversee a team of 10.Proven GMP and clinical trial operations experience.To apply, send your resume to
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