Clinical Trial Coordinator

Job Responsibilities

• Develop enrolment/follow-up mechanisms
• Enrolment and follow-up of study subjects
• Subject follow-up procedures
• Case report form (CRF) completion and study documentation
• Adverse event monitoring and reporting responsibilities
• Coordinate communications between internal and external stakeholders
• Manage regulatory documents
• Organise and coordinate study related meetings
• Assist in budget and agreement preparation, audit findings, monitor financial aspects for research projects/clinical trials

Job Requirements

• Diploma in Nursing, health sciences or para-clinical disciplines
• Possess working knowledge of applicable regulations and guidelines, e.g. SG-GCP, ICH-GCP, Code of Federal Regulations, Declaration of Helsinki, etc
• Proficient in Microsoft office