Research Assistant

Consortium for Clinical Research and Innovation Singapore; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A leading clinical research organization in Singapore is looking for a Research Assistant to support the IMR Self-Management Programme. You will partner with the research team to oversee project management and operations, while conducting recruitment and data analysis. Ideal candidates have a degree in health sciences and research competence. This role demands strong analytical skills and the ability to work independently as well as collaboratively. Continuous self-development is encouraged.

Qualifications

• Relevant competence in conducting research.
• Ability to build and maintain strong working relationships internally and externally.
• Self‑directed learner who embraces continuous learning and development.

Responsibilities

• Partner with the Principal Investigator and research team to achieve project deliverables.
• Oversee general project management and day-to-day operations at the study site.
• Maintain professional conduct and record keeping as per policies.

Skills

Research competence

Technical writing

Analytical skills

Communication skills

Proficiency in SPSS

Education

Degree in health sciences or related studies

Tools

SPSS

MS Office

Job description

Research Assistant (on effects of the IMR Self-Management Programme) (HSS/SG)

Singapore Institute of Technology – Punggol

As a University of Applied Learning, SIT works closely with industry in our research pursuits. Our research staff will be able to equip themselves with applied research skill sets relevant to industry demands while working on research projects at SIT.

Key Responsibilities

• Partner with the Principal Investigator, co-PI, and research team to achieve all project deliverables.
• Oversee general project management and conduct day‑to‑day operations at the study site, including recruitment, intervention provision, and data collection.
• Provide administrative and secretarial support, organize regular meetings, and maintain communication with study site collaborators.
• Perform literature searches, enter and analyze data using SPSS, maintain the trial database, and assist in preparing progress and final reports.
• Maintain professional conduct and record keeping per policies and procedures; assist with ethical application, amendments, and submission of annual and final reports.
• Carry out risk assessment and ensure compliance with Work, Safety and Health Regulations.
• Coordinate procurement and liaise with vendors/suppliers.
• Work independently and within a team to ensure proper operation and maintenance of equipment.
• Perform additional tasks as assigned.

Job Requirements

• Relevant competence in conducting research.
• Degree in health sciences or related studies.
• Knowledge of SPSS and MS Office is advantageous.
• Ability to build and maintain strong working relationships internally and externally.
• Self‑directed learner who embraces continuous learning and development.
• Proficient in technical writing and presentation.
• Strong analytical and critical thinking skills.
• Demonstrates strong initiative and ownership of work.