Clinical Research Coordinator (ACP Surgery)

SINGAPORE GENERAL HOSPITAL PTE LTD; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading healthcare institution is seeking a Clinical Research Coordinator to support the Surgery Academic Clinical Programme. The successful candidate will help manage and coordinate health services clinical research projects, ensuring compliance with protocols and regulations. Responsibilities include recruitment, data management, and liaising with stakeholders. Ideal candidates should possess a Bachelor's degree in a related field and relevant experience in clinical trials management.

Qualifications

• Bachelor's degree in biomedical sciences/Life Sciences/Nursing or related field required.
• At least 2 years of relevant experience in clinical trials management preferred.

Responsibilities

• Assist in planning, implementing, and coordinating clinical research studies.
• Conduct participant recruitment, screening, and obtain informed consent.
• Ensure compliance with ethical and regulatory requirements.
• Maintain study records and prepare reports.

Skills

Interpersonal skills

Communication skills

Attention to detail

Data management

Analytical skills

Education

Bachelor's degree in biomedical sciences/Life Science/Nursing or related fields

Tools

Microsoft Office

Job description

You will work in a clinical research setting, supporting the research team in the management and coordination of health services clinical research projects in Surgery Academic Clinical Programme (Surgery ACP)

You will be responsible for coordinating and implementing various health services clinical research studies in compliance with study protocols, good clinical practices, and regulatory requirements.

Job Responsibilities

• Assist in the planning, implementation, and coordination of clinical research studies, including preparing study documents, coordinating study visits, and managing study timelines.
• Conduct study participant recruitment and screening, obtaining informed consent, and collecting and recording study data accurately and efficiently.
• Ensure compliance with study protocols, good clinical practices, and regulatory requirements, including monitoring and reporting adverse events.
• Maintain study records and databases, and prepare study reports and presentations as required.
• Liaise with study sponsors, study sites, and other stakeholders to ensure effective communication and collaboration throughout the study.
• Ensure that all study-related activities are conducted in accordance with ethical, legal, and regulatory requirements.

Relevant Experience & Skills

· Bachelor's degree in biomedical sciences/Life Science/Nursing or related fields

· At least 2 years of relevant working experience in clinical trials management would be preferred

· Excellent interpersonal and communication (written and verbal) skills

· Strong attention to detail and accuracy

· Bilingual and/or knowledge of local dialects desired

· Proficiency in Microsoft Office applications

Qualities

· Ability to work independently and as part of a team

· Takes initiatives and is self-motivated

· Detail-oriented, with strong administrative, data management and analysis skills

· Able to multi-task and work efficiently with short deadlines