Clinical Research Associate II: Global Trials & Site Management

Emerald Clinical; Malaysia; Hybrid; MYR 85,000 - 120,000; Full time

Benefits offered by this job

Hybrid or remote work

Career growth

Wellbeing programs

Global opportunities

Job summary

Emerald Clinical Trials is seeking a Clinical Research Associate 2 to join our Clinical Operations team. You will oversee site management, perform monitoring activities, and provide regulatory support to ensure trials run on time, within scope, and in full compliance.

The ideal candidate holds a tertiary science or health care qualification and has at least two years of on-site monitoring experience in academic, CRO, or pharmaceutical settings.

Qualifications

• Tertiary qualification in a related science or health care discipline.
• Minimum 2 years on-site monitoring and site management experience in academic, CRO, or pharmaceutical environments.
• Renal and/or Oncology trial experience is a plus.
• Solid understanding of ICH-GCP guidelines and regulatory requirements.

Responsibilities

• Coordinate investigator and site identification, feasibility, and selection for trials.
• Complete monitoring activities per Monitoring Plan and prepare visit reports.
• Prepare, plan, and conduct site initiation visits and site evaluations.
• Prepare regulatory packages and liaise with regulatory colleagues; manage Ethics Committee submissions.

Skills

On-site monitoring

Site management

Regulatory knowledge

Negotiation skills

Communication

Education

Bachelor's degree in a related science or health care

Job description

Emerald Clinical Trials is seeking a Clinical Research Associate 2 to join our Clinical Operations team. You will oversee site management, perform monitoring activities, and provide regulatory support to ensure trials run on time, within scope, and in full compliance.

The ideal candidate holds a tertiary science or health care qualification and has at least two years of on-site monitoring experience in academic, CRO, or pharmaceutical settings.