Senior Lead Clinical Research Associate, Research Compliance Management

Singapore General Hospital; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A major healthcare institution in Singapore is seeking a Senior Lead Clinical Research Associate to ensure regulatory compliance across clinical trials. The ideal candidate will have at least 10 years of relevant experience, including 4 years in a management role, possessing strong leadership and communication skills. This role involves planning monitoring visits, preparing reports, and training new associates, contributing to high standards of clinical research management.

Qualifications

• At least 10 years of relevant experience in clinical trials, including clinical trials monitoring.
• 4 years in a supervisory or management role required.
• Strong interpersonal and leadership skills.

Responsibilities

• Planning and conducting monitoring visits.
• Preparing comprehensive post-visit reports.
• Recommending preventive and corrective measures for compliance.

Skills

Clinical trials monitoring

Leadership

Communication skills

Analytical skills

Problem-solving

Organisational skills

Tools

Microsoft Office

Job description

Overview

We are seeking a Senior Lead Clinical Research Associate to oversee clinical research compliance management across SingHealth institutions. In this role, you will ensure adherence to regulatory requirements including the Human Biomedical Research Act, Health Products Act, International Council for Harmonisation - Good Clinical Practice guidelines and relevant Standard Operating Procedures.

Responsibilities

• Planning and conducting monitoring visits
• Preparing comprehensive post-visit reports
• Recommending preventive and corrective measures for compliance
• Ensuring resolution of findings
• Providing administrative support to departmental operations
• Developing education programmes
• Training new Clinical Research Associates
• Providing supervisory monitoring and chairing department meetings

Qualifications

• At least 10 years of relevant experience in clinical trials, including clinical trials monitoring with 4 years in a supervisory or management role
• Strong interpersonal, leadership and communication skills (both verbal and written)
• Demonstrated analytical, problem-solving and organisational skills
• Ability to work independently and collaboratively, with proven capability to prioritise tasks and manage competing deadlines
• Proficiency with Microsoft Office applications