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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:
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.
- Recruitment Strategies: Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes
- 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.
- 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.