Clinical Research Associate 2

2 weeks ago

Singapore IQVIA Full time

Currently seeking Clinical Research Associate 2for our Sponsor-dedicated team. Step into a dynamic role where you’ll drive innovation and excellence in clinical research. As a key player in our team, you’ll ensure that study sites are not just compliant but thriving, contributing to groundbreaking advancements in healthcare.

When you join IQVIA Singapore as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.

With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.

You must have a minimum of 2 years Independent on-site monitoring experience to be considered for this role.

You will be asked to complete a short video screening as part of the interview process.

**Essential Functions**:

- ** Engage in Site Visits**: From selection to close-out, your visits will be pivotal in ensuring the success of our studies.
- ** Empower Sites with Knowledge**: Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
- ** Champion Quality and Integrity**: Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
- ** Drive Study Progress**: Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.
- ** Master Documentation**: Keep meticulous records and ensure all site documents are perfectly maintained.
- ** Collaborate and Innovate**: Work closely with a passionate team to support project execution and drive success.
- ** Manage Finances with Precision**: Oversee site financials and ensure timely invoice retrieval.

**Qualifications**:

- ** Educational Excellence**: Bachelor’s degree in a scientific or healthcare discipline preferred.
- ** Experience Matters**: At least 2years of on-site monitoring experience, with preference for Oncology trial management exposure.
- ** Regulatory Savvy**: Strong knowledge of GCP and ICH guidelines.
- ** Tech-Savvy**: Proficiency in Microsoft Office and relevant technology.
- ** Communication Pro**: Excellent written and verbal skills.
- ** Organized and Analytical**: Strong organizational and problem-solving abilities.
- ** Time and Financial Management**: Effective in managing time and finances.
- ** Team Player**: Ability to build and maintain strong relationships with coworkers, managers, and clients.

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