Clinical Research Associate

This is a fully remote position, open to applicants in Singapore.

📋 Description

• Perform site qualification, initiation, routine monitoring, and close-out visits.

• Ensure adherence to protocols and prioritize patient safety.

• Review source documentation and verify study data accuracy.

• Provide support to investigator sites throughout the entire clinical trial process.

• Manage relationships with sites and deliver training as necessary.

• Identify and escalate issues in a timely manner.

• Maintain high-quality documentation within study systems and the Trial Master File (TMF).

• Assist with recruitment and retention efforts.

• Join a talent pipeline for upcoming projects and resource needs as study awards and business demands arise.

⛳️ Requirements

• A degree in Life Sciences or a related healthcare field.

• At least 2 years of independent monitoring experience.

• Experience in CRO, academic research, or pharmaceutical settings.

• Strong understanding of ICH-GCP and European regulatory standards.

• Excellent communication skills with the ability to build relationships.

• Willingness to travel regionally.

• Preferred experience in renal, nephrology, cardiometabolic, or oncology studies.

🏝️ Benefits

• Competitive salary and benefits package tailored to your skills and experience.

• Options for hybrid or remote working arrangements, based on location and role.

• Opportunities for learning and access to a global network of scientific leaders.

• Employee wellbeing programs and initiatives that promote work-life balance, health, and team connectivity.

• Participation in global engagement surveys.

• Recognition programs to celebrate achievements.

• Team-building events to foster collaboration.

• Exposure to a variety of international projects and clients.