Clinical Research Associate/Clinical Operations Associate

KIMBERLEY CONSULTING PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A clinical research company in Singapore is seeking a Clinical Research Associate to manage clinical trials and support various operations. Candidates should have a Bachelor's in Life Sciences and 2-5 years' experience in clinical research. This role offers a competitive salary, hands-on environment, and growth opportunities in clinical operations and project management.

Benefits

Competitive salary

Benefits package

Growth opportunities

Qualifications

• 2–5 years of experience in clinical research or operations.
• Practical experience in site monitoring and understanding of ICH-GCP.
• Organized, meticulous, and proactive.

Responsibilities

• Manage and execute clinical trials in Singapore.
• Conduct site monitoring visits and document findings.
• Coordinate ethics submissions and regulatory applications.
• Track timelines and procurement activities.

Skills

Site monitoring

Documentation

Project management

Communication

Education

Bachelor’s degree in Life Sciences

Job description

Overview

Our client is expanding their clinical operations team and is looking for a Clinical Research Associate / Clinical Operations Associate to support the planning and execution of ongoing and upcoming clinical studies. The head office is based in the United States, with a Singapore clinical research branch established in the western region of Singapore.

Responsibilities

• Support day-to-day management and execution of clinical trials in Singapore
• Conduct and document site monitoring visits (pre-study, initiation, routine, and close-out)
• Assist in the development of trial protocols, CRFs, and related study documentation
• Coordinate ethics submissions and regulatory applications (IRB / HSA)
• Track investigational product and trial materials to ensure compliance with GCP and SOPs
• Provide project management support — tracking timelines, vendors, and procurement activities
• Collaborate closely with internal scientists, regulatory staff, and external clinical partners
• Oversee coordination of project extensions with the CRO, facilitating communication between the Singapore and US headquarters, research centres, hospitals and pharmaceutical stakeholders

Requirements

• Bachelor’s degree in Life Sciences, Medical Sciences, or related field
• 2–5 years of experience in clinical research, clinical operations, or trial coordination
• Practical experience in site monitoring and strong understanding of ICH-GCP
• Organized, meticulous, and proactive with excellent documentation habits
• Clear communicator with the ability to work independently in a small, agile team
• Exposure to project or program management is a plus

Why Join Us

• Be part of a mission-driven biotech tackling rare diseases from Singapore
• Work in a hands-on, cross-functional environment where your contributions matter
• Competitive salary and benefits package
• Growth opportunities into clinical operations, project management, or regulatory pathways