[URGENT] Clinical Research Project Specialist (Clinical Trial)

TALENT TRADER GROUP PTE. LTD.; Singapore; Sur place; SGD 90 000 - 130 000; Plein temps

Avantages offerts par ce poste

Good Employee Benefits

Attractive Salary Package

Résumé du poste

TALENT TRADER GROUP PTE. LTD. is seeking a Clinical Research Coordinator to manage end-to-end trial activities. You will coordinate start-up, execution, and close-out phases, liaising with sponsors, vendors, monitors and ethics committees.

The role requires at least 5 years in clinical research, strong GCP knowledge, and meticulous documentation. Based in Singapore, the position focuses on regulatory submissions, risk mitigation and cross-functional communication.

Qualifications

• Diploma or Degree in Nursing, Science, Healthcare, Health Management or related field.
• Minimum 5 years of clinical research experience, preferably with Clinical Research Unit / Phase 1 operations.
• Strong knowledge of Good Clinical Practice (GCP) and clinical trial processes.

Responsabilités

• Manage clinical trial activities from study start-up through close-out.
• Coordinate study implementation, timelines, milestones and deliverables.
• Liaise with sponsors, study teams, monitors, ethics committees and external vendors.
• Review and coordinate study-related documents and trial materials.
• Support study risk assessment and implementation of mitigation plans.
• Coordinate site training, study initiation, monitoring and close-out visits.
• Lead study meetings and ensure effective communication among stakeholders.
• Track study progress and provide regular updates on status, issues and timelines.
• Coordinate regulatory and ethics submission requirements.
• Support subject safety reporting and follow-up on study-related issues.
• Coordinate resolution of protocol, data and monitoring queries.
• Maintain accurate and complete clinical trial documentation and records.
• Coordinate study supplies, logistics and external vendors.
• Support study budget tracking and financial administration.
• Ensure study activities comply with GCP, SOPs and applicable regulatory requirements.
• Support audits, inspections and quality-related activities.
• Contribute to process improvements and study lessons-learned activities.
• Support archival and close-out of study documentation.
• Travel when required for study-related activities.

Connaissances

GCP knowledge

Clinical research

Formation

Nursing/Healthcare degree

Description du poste

Benefits

Good Employee Benefits
Attractive Salary Package

Responsibilities

• Manage clinical trial activities from study start-up through close-out.
• Coordinate study implementation, timelines, milestones and deliverables.
• Liaise with sponsors, study teams, monitors, ethics committees and external vendors.
• Review and coordinate study-related documents and trial materials.
• Support study risk assessment and implementation of mitigation plans.
• Coordinate site training, study initiation, monitoring and close-out visits.
• Lead study meetings and ensure effective communication among stakeholders.
• Track study progress and provide regular updates on status, issues and timelines.
• Coordinate regulatory and ethics submission requirements.
• Support subject safety reporting and follow-up on study-related issues.
• Coordinate resolution of protocol, data and monitoring queries.
• Maintain accurate and complete clinical trial documentation and records.
• Coordinate study supplies, logistics and external vendors.
• Support study budget tracking and financial administration.
• Ensure study activities comply with GCP, SOPs and applicable regulatory requirements.
• Support audits, inspections and quality-related activities.
• Contribute to process improvements and study lessons-learned activities.
• Support archival and close-out of study documentation.
• Travel when required for study-related activities.

Requirements

• Diploma or Degree in Nursing, Science, Healthcare, Health Management or related field.
• Minimum 5 years of clinical research experience, preferably with Clinical Research Unit / Phase 1 operations.
• Strong knowledge of Good Clinical Practice (GCP) and clinical trial processes.