Clinical Research Associate

About Emerald Clinical

Emerald Clinical Trials is a globally recognized leader in clinical research, collaborating with over 160 biotechnology firms and 15 of the top 20 pharmaceutical companies worldwide. Based in Singapore, the company excels in scientific precision and operational proficiency, delivering comprehensive clinical trial services covering Phase I to IV and real-world studies. With more than 25 years of expertise and a specialized focus on renal disease research, Emerald Clinical has contributed significantly to medical advancements through deep scientific knowledge, precise execution, and a steadfast commitment to quality.

Operating internationally with over 800 staff members across Asia-Pacific, Europe, and the Americas, the company leverages local insights and global reach to accelerate recruitment, enhance patient engagement, and generate impactful clinical outcomes.

Role Overview

The Clinical Research Associate 2 (CRA2) role is integral to the Clinical Operations division, which manages clinical trial sites, monitoring, and operational support, ensuring adherence to regulatory standards and internal Standard Operating Procedures (SOPs). The role involves resource allocation and active participation in executing project plans.

Key Responsibilities

• Coordinate processes for identifying, assessing feasibility, and selecting investigators and trial sites.
• Conduct monitoring visits per the Monitoring Plan, complete thorough visit reports accurately and within deadlines.
• Organize and perform site evaluations and report findings to aid site selection decisions.
• Collaborate with regulatory specialists to prepare regulatory submissions, import/export logistics, and ethics committee documentation.
• Negotiate site budgets, manage contract execution, monitor invoicing, and ensure prompt payments to sites.
• Plan and carry out site initiation visits effectively.
• Maintain and develop monitoring tools and project documentation specific to each trial.
• Train and motivate site personnel on protocol adherence, investigational products, and trial requirements to fulfill trial obligations accurately and punctually.
• Collect, review, and approve critical documents from trial sites, ensuring compliance and quality, and manage Trial Master File (TMF) documentation.
• Reconcile documentation between internal TMF and Investigator Site Files.
• Manage distribution, tracking, handling, and proper destruction of investigational products and supplies per trial requirements.
• Update clinical trial management systems and maintain accurate trial data and reporting tools.
• Support and implement recruitment enhancement strategies.

Candidate Profile

• Educational background in a scientific or healthcare-related field.
• Prior experience in clinical trials in academic, CRO, or pharmaceutical settings, with 2 to 5 years of on-site monitoring and site management experience.
• Exposure to oncology and/or early-phase clinical trials is advantageous.
• Strong understanding of ICH-GCP guidelines and compliance with global and local ethical and regulatory standards.
• Proficient in ethical considerations, participant safety, site management (start-up and ongoing), risk and quality management, supply chain oversight, clinical research design, and issue escalation protocols.
• Skilled in negotiation, conflict resolution, critical thinking, decision-making, and strategic planning.
• Excellent communication, presentation capabilities, and ability to collaborate within multidisciplinary teams and with diverse stakeholders.
• Adaptable and flexible to shifting organizational priorities and dynamic environments.
• Willing and able to travel as required.

Why Join Emerald Clinical?

Emerald Clinical Trials prioritizes both patient well-being and employee development. As part of this global community of committed professionals, you will contribute to clinical research that meaningfully improves health outcomes worldwide.

Company Highlights

• Engage in purpose-driven work focusing on renal, cardiometabolic, and oncology therapies.
• Benefit from global presence combined with in-depth local knowledge that fosters community trust and patient engagement.
• Collaborate in an innovative culture that values diversity, creativity, and solving global health challenges.

Employee Benefits

• Competitive salary and comprehensive benefits tailored to skills and experience.
• Flexible working options including hybrid and remote setups where applicable.
• Opportunities for professional growth through learning programs and global scientific networks.
• Support for employee well-being via work-life balance initiatives, health programs, recognition, and team events.
• Access to a broad array of international projects and clients, enriching your professional experience.

Emerald Clinical is an equal opportunity employer and welcomes applications from all qualified individuals.