Senior / Clinical Research Associate (Client Dedicated)

IQVIA Argentina; Singapore; On-site; SGD 60,000 - 80,000; Full time

Benefits offered by this job

Career development opportunities

Flexible work schedules

Attractive remuneration package

Job summary

IQVIA Argentina is seeking a Senior Clinical Research Associate (CRA) in Singapore. This role offers the opportunity to manage site selection, monitoring, and improve clinical practice quality.

The ideal candidate will have at least a year of on-site monitoring experience and a degree in a scientific or healthcare field. The company promotes professional growth, flexible work arrangements, and offers an attractive remuneration package.

Qualifications

• Minimum 1 year of on-site monitoring experience.
• Good knowledge of GCP and clinical research regulatory requirements.
• Excellent command of English.

Responsibilities

• Perform site selection, initiation, monitoring and close‑out visits.
• Support development of a subject recruitment plan.
• Evaluate the quality and integrity of site practices.

Skills

On-site monitoring experience

Knowledge of GCP

Organizational skills

Problem-solving skills

Education

University degree in a scientific discipline or healthcare

Job description

Overview

As you develop your career as a Senior CRA or CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a ‘career ceiling.’ You will be exposed to wider opportunities like operations management, dedicated customer solutions, project management and more. You will have dedicated mentoring and receive structured quarterly reviews on performance, promotion opportunities and awards. Joining IQVIA will give you access to cutting‑edge in‑house technology and opportunities to work on global projects and trials, building a flexible, meaningful and fulfilling career with no limits.

Key Responsibilities

• Perform site selection, initiation, monitoring and close‑out visits, maintaining appropriate documentation.
• Support development of a subject recruitment plan.
• Establish regular lines of communication and administer protocol and related study training to assigned sites.
• Evaluate the quality and integrity of site practices, escalating quality issues as appropriate.
• Manage progress by tracking regulatory submissions, recruitment, case report form (CRF) completion and data query resolution.
• Collaborate and communicate with a variety of colleagues and customers, applying good knowledge of applicable clinical research regulatory requirements.

Qualifications

• University degree in a scientific discipline or healthcare.
• At least 1 year of on‑site monitoring experience.
• Good knowledge of GCP and clinical research regulatory requirements.
• Excellent command of English language.
• Organizational, time‑management and problem‑solving skills.
• Ability to establish and maintain effective working relationships with colleagues, managers and customers.
• Flexibility to travel.

What You Can Expect

• Working with different customers on global trials.
• Career development opportunities for those passionate about growing within the organization.
• Supportive leaders who endorse flexible work schedules and arrangements.
• Excellent working environment in a stable, international, reputable company.
• Programs to build technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape.
• Attractive remuneration package.