Clinical Research Coordinator (NUHCS)

National University Health System; Singapore; In loco; SGD 28.000 - 42.000; Tempo pieno

Descrizione del lavoro

National University Health System (NUHS) is seeking a dedicated research support professional to coordinate study activities, recruit participants, collect data, and maintain meticulous documentation in accordance with IRB, GCP, and PDPA standards.

You will work under the research team manager, ensuring data confidentiality and smooth day-to-day operations in a clinical setting, engaging with patients, and supporting administrative tasks.

Competenze

• Good communication and interpersonal skills with patients
• Meticulous, organised and able to handle confidential information
• Proficient in Microsoft Office and basic data entry tools
• Ability to work independently and collaboratively in a clinical environment

Mansioni

• Assist the research team in implementing research protocols and workflows
• Approach, screen, and recruit eligible patients according to study protocols
• Collect clinical data and ensure data completeness, accuracy, and confidentiality in accordance with PDPA and institutional policies
• Support preparation of study documents and assist with related administrative and logistics tasks
• Ensure all study activities comply with IRB, SOPs, GCP standards, and regulatory requirements

Conoscenze

Communication skills

Interpersonal skills

Meticulous

Organised

Confidentiality handling

Independent and collaborative work

Proficient in Microsoft Office

Formazione

Degree/Diploma in Life Sciences, Nursing, Allied Health, or related fields

Strumenti

Microsoft Office

Data entry tools

Descrizione del lavoro

Reporting to the research team manager, you will support research studies by coordinating study activities, collecting clinical data, conducting patient interviews, ensuring proper documentation, and assisting in day-to-day study operations according to institutional and regulatory requirements.

Roles and Responsibilities

• Assist the research team in implementing research protocols and workflows
• Approach, screen, and recruit eligible patients according to study protocols
• Collect clinical data and ensure data completeness, accuracy, and confidentiality in accordance with PDPA and institutional policies
• Support preparation of study documents and assist with related administrative and logistics tasks
• Ensure all study activities comply with Institutional Review Board (IRB), institutional SOPs, Good Clinical Practice (GCP) standards, and regulatory requirements

Requirements

• Degree/Diploma in Life Sciences, Nursing, Allied Health, or related fields
• Prior research or clinical experience will be an advantage but not mandatory. Fresh graduates are welcome
• Good communication and interpersonal skills, especially with patients
• Meticulous, organised, and able to handle confidential information responsibly
• Proficient in Microsoft Office and basic data entry tools
• Ability to work independently and collaboratively in a clinical environment