(Senior) Clinical Research Associate

IQVIA Argentina; Petaling Jaya; On-site; MYR 48,000 - 72,000; Full time

Job summary

An established industry player offers an exciting opportunity for a Senior Clinical Research Associate (CRA) to advance their career without limits. In this dynamic role, you will engage in global projects, ensuring high-quality clinical trials while collaborating with diverse teams. You'll enjoy structured mentoring, career development opportunities, and a supportive work environment that values flexibility. With access to cutting-edge technology and a commitment to professional growth, this position is ideal for those passionate about making a meaningful impact in the healthcare sector. Join a reputable organization that prioritizes your career aspirations and offers an attractive remuneration package.

Benefits

Career Development Opportunities

Flexible Work Schedules

Supportive Working Environment

Technical Skills Programs

Attractive Remuneration Package

Qualifications

• 1+ year of on-site monitoring experience in clinical research.
• Strong knowledge of GCP and regulatory requirements.

Responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits.
• Manage regulatory submissions and data query resolution.

Skills

Monitoring Experience

Communication Skills

Organizational Skills

Problem-Solving Skills

Time Management

Knowledge of GCP

Flexibility to Travel

Education

University Degree in Scientific Discipline

Healthcare Degree

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.

Your responsibilities will include:

1. Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation.
2. Supporting the development of a subject recruitment plan.
3. Establishing regular lines of communication plus administering protocol and related study training to assigned sites.
4. Evaluating the quality and integrity of site practices – escalating quality issues as appropriate.
5. Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.
6. 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:

1. University degree in scientific discipline or healthcare.
2. At least 1 year of on-site monitoring experience.
3. Good knowledge of GCP and clinical research regulatory requirements.
4. Good computer skills including MS Office.
5. Excellent command of English language.
6. Organizational, time management and problem-solving skills.
7. Ability to establish and maintain effective working relationships with colleagues, managers, and customers.
8. Flexibility to travel.

What you can expect:

1. Working with different customers on global trials.
2. Career development opportunities for those who are passionate in wanting to grow as part of the organization.
3. Leaders that support flexible work schedules/arrangement.
4. Excellent working environment in a stable, international, reputable company.
5. Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape.
6. Attractive remuneration package.