Senior / Clinical Research Associate

IQVIA RDS EAST ASIA PTE. LTD.; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A leading clinical research organization is seeking a Senior CRA in Singapore. The role focuses on site selection, monitoring, and maintaining documentation for clinical trials. Candidates should have a university degree in a scientific discipline or healthcare, with at least 1 year of on-site monitoring experience. Strong communication skills and the ability to manage relationships with stakeholders are essential. The position offers career development opportunities, flexible work schedules, and a competitive remuneration package.

Benefits

Career development opportunities

Flexible work schedules

Attractive remuneration package

Access to in-house technology

Qualifications

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

Responsibilities

• Perform site selection, initiation, monitoring, and close-out visits.
• Support the development of a subject recruitment plan.
• Manage regulatory submissions, recruitment, and data queries.

Skills

On-site monitoring

Good communication

Ability to build relationships

Organizational skills

Problem-solving

Time management

Education

University degree in scientific discipline or healthcare

Tools

MS Office

Job description

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. And you won’t do it alone – 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 provide opportunities to work on global projects/ trials. You will be building a flexible, meaningful and fulfilling career with no limits.

Responsibilities

• Performing site selection, initiation, monitoring, and close‑out visits, plus maintaining appropriate documentation
• Supporting the development of a subject recruitment plan
• Establishing regular lines of communication plus administering protocol and related study training to assigned sites
• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
• You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You will need to have a good knowledge of applicable clinical research regulatory requirements.

Qualifications

• University degree in scientific discipline or healthcare
• At least 1 year of on‑site monitoring experience
• Good knowledge of GCP and clinical research regulatory requirements
• Good computer skills including MS Office
• 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 who are passionate in wanting to grow as part of the organization.
• Leaders that support flexible work schedules/arrangement
• Excellent working environment in a stable, international, reputable company
• Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape
• Attractive remuneration package.