Senior Clinical Research Associate - Global Trials

Emerald Clinical Trials Inc.; Singapore; On-site; SGD 70,000 - 110,000; Full time

Benefits offered by this job

Competitive Compensation

Hybrid or remote working arrangements

Career Growth

Employee Wellbeing

Global Opportunities

Job summary

Emerald Clinical Trials in Singapore is seeking a Senior Clinical Research Associate (SCRA) to join the Clinical Operations group. You will manage site selection, initiation, monitoring, and close-out visits, ensuring study documents and SOPs are followed and GCP requirements are met.

Candidates should hold a bachelor’s degree in a health-related field, have at least five years of trial monitoring experience (nephrology or oncology preferred), and be proficient in standard office software.

Qualifications

• Bachelor’s degree or above in a medicine/health-related discipline.
• Minimum of 5 years of clinical trial monitoring experience; nephrology/oncology experience preferred.
• Strong learning, organizational and coordination skills; excellent written and verbal communication.
• High level of integrity and solid execution capabilities.
• Proficient in standard office software applications.
• CET-6 or equivalent English proficiency with fluent reading and writing.

Responsibilities

• Conduct study site selection, initiation, monitoring, close-out visits and study documents management in accordance with trial protocol, SOPs and GCP requirements.
• Comply with regulatory requirements and SOPs; ensure quality and timely data.

Skills

Clinical monitoring

Site management

Coordination

Communication skills

Integrity

Education

Bachelor’s degree or above in a medicine/health-related discipline

Tools

Office software

Job description

Emerald Clinical Trials in Singapore is seeking a Senior Clinical Research Associate (SCRA) to join the Clinical Operations group. You will manage site selection, initiation, monitoring, and close-out visits, ensuring study documents and SOPs are followed and GCP requirements are met.

Candidates should hold a bachelor’s degree in a health-related field, have at least five years of trial monitoring experience (nephrology or oncology preferred), and be proficient in standard office software.