Coordinator

Tan Tock Seng Hospital; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading medical institution in Singapore is seeking a dedicated individual to assist in clinical research activities. The role involves supporting Principal Investigators, managing research data, and ensuring compliance with ethical standards. Candidates should possess at least 'O' or 'N-level' education and demonstrate proficiency in English and Mandarin. Working experience in academic or clinical research is preferred. Strong communication, organisational, and multitasking skills are essential for success in this dynamic environment.

Qualifications

• Working experience in academic or clinical research would be advantageous.
• Proficient in English and Mandarin; proficiency in Malay and Tamil will be an added advantage.
• Knowledge in research ethics and preferably completed the CITI.

Responsibilities

• Assist and support Principal Investigators in clinical research activities.
• Annotation of radiology images.
• Manage data entry, data cleaning, and ethics/legal compliance.
• Liaise with relevant internal and external agencies.
• Monitor financial aspects of assigned study and advise the PI.
• Ensure timely submission of progress reports.
• Undertake other tasks assigned by the Supervisor.

Skills

Working experience in academic or clinical research

Proficient in English and Mandarin

Good written and oral communication skills

Team-oriented

Strong coordination and organisational skills

Able to work independently

Multitasking skills

Education

‘O’ or ‘N-level’ or equivalent

Tools

MS Word

MS Excel

Power Point

Outlook

Job description

Family Group: Allied Health

Roles and Responsibilities

1. Assist and support Principal Investigators (PI) in their clinical research activities injury law involved from study start‑up till study end including study closure activities.
2. Annotation of radiology images.
3. Manage researchLeftRight, data entry, data cleaning and ethics/legal compliance.
4. Liaise with relevant internal and external agencies during the course of work.
5. Monitor the financial aspects of the assigned study and advise the PI.
6. Ensure timely submission of progress reports to the relevant agencies and authorities and renewal of ECOS approvals.
7. Undertake any other tasks assigned by the Supervisor.

Requirements

1. ‘O’ or ‘N-level’ or equivalent.
2. Working experience in academic or clinical research would be advantageous.
3. Proficient in English and Mandarin; proficiency in Malay and Tamil will be an added advantage.
4. Proficient in MS Word, MS Excel, Power Point and Outlook.
5. Knowledge in researchKode ethics and preferably completed the CITI.
6. Good written and oral communication skills.
7. Team‑oriented with strong coordination and organisational skills.
8. Able to work independently and comfortable to multi‑task / handle a few projects concurrently.