Clinical Research Coordinator (Contract)

Singapore National Eye Centre; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator to support clinical trials and research projects. In this role, you will assist Principal Investigators in ensuring compliance with Singapore Good Clinical Practice (GCP) guidelines, organizing and coordinating study workflows, and maintaining proper documentation. Your strong organizational skills and ability to communicate effectively will be essential in managing patient queries and collaborating with regulatory bodies. This is a fantastic opportunity to contribute to impactful research in a dynamic environment.

Qualifications

• Degree in Life Science or Nursing required.
• 2 years experience in clinical research preferred.

Responsibilities

• Assist in conducting clinical trials according to GCP guidelines.
• Coordinate workflow of study projects from initiation to completion.

Skills

Clinical Research Coordination

Organizational Skills

Communication Skills

Education

Life Science Degree

Nursing Degree

Nursing Diploma with Experience

Job description

Clinical Research Coordinator (Contract)

Job Category: Administration

Posting Date: 21 Mar 2025

Job Description: You will assist Principal investigators in conducting clinical trials & research projects according to Singapore Good Clinical Practice (GCP) guidelines. You will plan, organise & coordinate workflow of study projects from initiation to completion phase, perform screening and recruitment activities as well as compile relevant patients' data and maintain proper study documentation according to established protocols and regulatory requirements. Additionally, you will facilitate coordination of research studies with funding and regulatory bodies. Other duties include providing administrative support for Research Department when the need arises.

Requirements:

• Life Science or Nursing Degree holder. Candidates with Nursing Diploma must have minimum 2 years of relevant experience.
• At least 1-2 years of experience in clinical research coordination.
• Ability to converse in mainstream languages (able to speak in local dialects will be an added advantage) to handle patient queries on the research study.
• Strong organizational skills, able to work independently and/or a team player, meticulous in details.