Senior Lead Clinical Research Associate, Research Compliance Management

Singapore National Eye Centre; Singapore; On-site; USD 80,000 - 120,000; Full time

Job summary

An established industry player is seeking a Senior Lead Clinical Research Associate to manage compliance in clinical research across various institutions. This pivotal role involves ensuring adherence to regulatory standards and conducting monitoring visits. The ideal candidate will have over a decade of experience in clinical trials, including supervisory responsibilities. Strong leadership and communication skills are essential, as you will train new associates and chair departmental meetings. Join a forward-thinking organization committed to excellence in research compliance and make a significant impact in the field.

Qualifications

• 10+ years of experience in clinical trials, with 4+ years in a supervisory role.
• Strong leadership, communication, and problem-solving skills.

Responsibilities

• Oversee clinical research compliance management across institutions.
• Plan and conduct monitoring visits, prepare post-visit reports.

Skills

Clinical Trials Monitoring

Regulatory Compliance

Leadership Skills

Analytical Skills

Communication Skills

Problem-Solving Skills

Organisational Skills

Tools

Microsoft Office

Job description

Press Tab to Move to Skip to Content Link

Select how often (in days) to receive an alert:

Senior Lead Clinical Research Associate, Research Compliance Management

Job Category: Allied Health Professional

Posting Date: 9 May 2025

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.

Your responsibilities will include planning and conducting monitoring visits, preparing comprehensive post-visit reports, recommending preventive and corrective measures for compliance, and ensuring resolution of findings. You will also provide administrative support to departmental operations, develop education programes, train new Clinical Research Associates, provide supervisory monitoring and chair department meetings.

Requirements:

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