Global Clinical Trials Project Lead

Emerald Clinical Trials Inc.

Singapore

Hybrid

SGD 90,000 - 140,000

Full time

38 hours ago
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Job summary

Emerald Clinical Trials in Singapore seeks a Project Manager to lead the development, conduct and completion of research projects in line with client requirements and GCP. You will oversee cross-functional teams, budgeting, timelines and regulatory compliance, mentoring junior staff and ensuring high-quality data and collaboration with sites and vendors.

The role requires strong communication with sponsors, meticulous documentation, and ability to drive projects from start-up through close-out,

Responsibilities

  • All activities must be conducted in accordance with project specific documentation, applicable SOPs, ICH GCP and applicable regulatory requirements.
  • Maintain effective professional relationships with external customers, investigators and vendors.
  • Maintain effective professional relationships with internal project team including those providing academic input.
  • Provide clear guidance to project team on project specific deliverables.
  • Project Kick-off: attend relevant project meetings, develop project plan and documents, coordinate feasibility planning and site selection, identify outsourcing needs.
  • Project Implementation and Closure: manage budgets, track scope, forecast invoicing, coordinate site feasibility and setup, monitor progress and milestones, ensure data quality and timely reporting.
  • Study Start-up: coordinate feasibility planning and site establishment, ensure ethics and regulatory submissions, develop trial management systems, training and site readiness.
  • Study Close-out: coordinate close-out visits, ensure reconciliation of supplies and archiving of documents, finalize reporting.
  • Data Management: ensure data completeness, quality, and timely queries resolution, adherence to protocol and ICH-GCP.

Job description

Emerald Clinical Trials in Singapore seeks a Project Manager to lead the development, conduct and completion of research projects in line with client requirements and GCP. You will oversee cross-functional teams, budgeting, timelines and regulatory compliance, mentoring junior staff and ensuring high-quality data and collaboration with sites and vendors.

The role requires strong communication with sponsors, meticulous documentation, and ability to drive projects from start-up through close-out,

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