Project Manager - Clinical Research

RECRUIT LYNC PTE. LTD.; Singapore; Presencial; SGD 60.000 - 90.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Completion Bonus

Buona Vista

Descripción de la vacante

RECRUIT LYNC PTE. LTD. in Singapore is seeking a Clinical Research Coordinator to lead planning, coordination and execution of studies.

You will serve as the liaison between the Clinical Research Unit, sponsors, and cross-functional teams to ensure timelines and deliverables are met. You will participate in protocol reviews, assist in study planning, monitor metrics, and drive process improvements while coaching the team to achieve operational objectives.

Formación

• Minimum Degree in Nursing, Sciences, Health related or Management field.
• Minimum 5 years of Clinical Research Coordination Experience.

Responsabilidades

• Lead the planning, coordination and execution of clinical research studies.
• Serve as the key point of contact between the Clinical Research Unit, sponsors and cross-functional study teams.
• Coordinate study activities, timelines, milestones and deliverables to ensure smooth execution.
• Provide operational input during study planning and support resolution of study-related issues.
• Ensure study activities comply with internal procedures, local regulatory and IRB requirements.
• Participate in protocol reviews, study meetings and operational discussions.
• Monitor study metrics, key actions and project documentation.
• Identify process improvements and share lessons learned to improve study execution.
• Lead, coach and manage team members to deliver operational objectives.

Educación

Minimum Degree in Nursing, Sciences, Health related or Management field

Descripción del empleo

• Monday - Friday
• Completion Bonus
• Buona Vista

Key Responsibilities

• Lead the planning, coordination and execution of clinical research studies.

• Serve as the key point of contact between the Clinical Research Unit, sponsors and cross-functional study teams.

• Coordinate study activities, timelines, milestones and deliverables to ensure smooth execution.

• Provide operational input during study planning and support resolution of study-related issues.

• Ensure study activities comply with internal procedures, local regulatory and IRB requirements.

• Participate in protocol reviews, study meetings and operational discussions.

• Monitor study metrics, key actions and project documentation.

• Identify process improvements and share lessons learned to improve study execution.

• Lead, coach and manage team members to deliver operational objectives.

Requirements:

• Minimum Degree in Nursing, Sciences, Health related or Management field
• Minimum 5 years of Clinical Research Coordination Experience

We regret to inform you that only shortlisted candidates will be notified.