Clinical Research Coordinator, PRISM (Contract)

Singapore Health Services Pte Ltd (SingHealth HQ); Singapore; On-site; SGD 42,000 - 65,000; Full time

Job summary

PRISM, the SingHealth Duke-NUS Institute of Precision Medicine, seeks a Clinical Research Coordinator to provide research and administrative support for clinical trials. You will ensure compliance with Singapore Guidelines for Good Clinical Practice and study protocol requirements while supporting investigators and collaborating across institutions.

You will help screen participants, obtain consent, coordinate visits, and manage data and study documentation, including reports for grant agencies

Qualifications

• Bachelor's Degree or Diploma in Life Sciences, Biology, Genomics, Nursing, or a related field.
• Prior clinical research experience is not required, though it would be an advantage.
• Strong written and verbal communication skills in English, including business writing.
• Good interpersonal skills and comfort in interacting with patients.
• Meticulous, self-motivated, able to work independently and as part of a team.
• Ability to manage multiple ongoing priorities effectively.

Responsibilities

• Support the full lifecycle of clinical research studies.
• Assist investigators in drafting and amending study protocols, informed consent forms, and other documents for IRB approval.
• Prepare study materials such as case report forms and questionnaires; liaise with investigators on collaborations.
• Screen potential participants, obtain informed consent, and coordinate participant visits.
• Enter and securely manage participant data in compliance with applicable laws.
• Assist in data management and reporting for grant agencies and regulators.
• Track study invoices and expenses; organize meetings and record minutes.

Skills

English writing

Interpersonal skills

Multitasking

Teamwork

Education

Bachelor's Degree in Life Sciences

Diploma in Life Sciences

Job description

Join PRISM, the SingHealth Duke-NUS Institute of Precision Medicine, and play a meaningful role in advancing genomic and precision medicine research. At PRISM, you will be part of a team dedicated to translating cutting-edge science into better health outcomes. We are looking for a Clinical Research Coordinator to provide research and administrative support to ensure the smooth conduct of clinical trials, and that work is carried out in adherence to the Singapore Guidelines for Good Clinical Practice and study protocol requirements.

What You Will Do:

You will support the full lifecycle of clinical research studies. This includes assisting investigators in drafting and amending study protocols, participant information sheets and consent forms, and other study documents for Central Institutional Review Board approval. You will also help prepare study materials such as case report forms and questionnaires, and liaise with investigators from other institutions on collaborative projects. On the clinical side, you will screen potential participants, obtain informed consent, and coordinate participant visits. You will enter and securely manage participant phenotype and personal data in accordance with the Human Biomedical Research Act and other relevant regulations. Your role extends to data management and reporting, assisting investigators in compiling clinical and periodic study reports for submission to grant agencies and regulators, as well as supporting data collection and analysis. You will also take on administrative responsibilities such as tracking study invoices and expenses, as well as organising meetings and recording minutes.

Job Requirements:

• Bachelor's Degree or Diploma in Life Sciences, Biology, Genomics, Nursing, or a related field

• Prior clinical research experience is not required, though it would be an advantage

• Strong written and verbal communication skills in English, including business writing

• Good interpersonal skills and comfort in interacting with patients

• Meticulous, self-motivated individual, with the ability to work both independently and as part of a team

• Ability to manage multiple ongoing priorities effectively