Clinical Research Associate / Clinical Operations Associate

Roles & Responsibilities

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.

Key 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
• Oversaw coordination of project extensions with the CRO, facilitating communication between the Singapore and US headquarters, research centres, hospitals and pharmaceutical stakeholders

Requirements :

Why Join Us

Tell employers what skills you have

Clinical Research Associate

Budgets

Hospitals

Clinical Research

CRO

Ability To Work Independently

Site Management

Clinical Operations

Clinical Trials

Protocol

Procurement

Program Management

Project Management

GCP

Life Sciences

Clinical Monitoring