Clinical Research Associate II
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| Company Name | Fortrea |
| Company Type | Private |
| Job Type | Full-Time |
| Salary Range | Market Competitive |
| Location | Singapore |
| Qualifications | Bachelor’s Degree |
| Experience | No Experience / Fresh |
Job Overview
Fortrea is seeking a Clinical Research Associate II to join their team in Singapore. This role involves contributing to innovative clinical development solutions within the life sciences industry, ensuring operational excellence and scientific rigor in clinical trials and advancing global health.
Company Overview
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) with over 30 years of experience, providing innovative clinical development solutions to the life sciences industry. Evolved from Covance and Labcorp, Fortrea specializes in full-service (FSO), functional service (FSP), and hybrid solutions, backed by deep experience in over 20 therapeutic areas. Operating in approximately 100 countries, Fortrea’s diverse and talented team ensures predictability in clinical trial execution and helps transform aspirations into outcomes. Learn more at Fortrea.com.
Quick Details
- Salary Range: Market Competitive
- Job Type: Full-time
- Qualifications: Bachelor’s Degree
- Experience: No Experience / Fresh
Key Responsibilities
- Assist in the execution of clinical trials according to protocol, GCP, and regulatory requirements.
- Monitor study sites for compliance, data integrity, and patient safety.
- Document and report findings from site visits and interactions promptly.
- Support site activation and close-out activities effectively.
- Collaborate with study teams to ensure efficient clinical trial progress.
- Maintain accurate and up-to-date trial documentation and records.
Requirements
- Bachelor’s degree in a life science or health-related field.
- Strong understanding of ICH-GCP guidelines and clinical trial regulations.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a collaborative team.
- Proficiency in Microsoft Office Suite and relevant clinical trial systems.
- Willingness to travel for site monitoring visits as required.
Benefits
- Opportunity to work with a leading global clinical research organization.
- Clear career development and growth opportunities within the life sciences industry.
- Exposure to diverse therapeutic areas and innovative solutions.
- Collaborative and supportive international work environment.
- Competitive compensation and benefits package.
- Contribution to transforming aspirations into outcomes in healthcare.