Clinical Research Associate
hace 4 semanas
Job Overview
At IQVIA, we are seeking a skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for conducting site monitoring visits to ensure that sites are conducting studies and reporting data as required by the study protocol, applicable regulations, and sponsor requirements.
Key Responsibilities
- Perform site monitoring visits to ensure compliance with study protocols and regulatory requirements.
- Work with sites to adapt and drive subject recruitment plans to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication.
- Evaluate the quality and integrity of study site practices and escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, and data query generation and resolution.
Qualifications
- Bachelor's Degree in a scientific discipline or healthcare preferred.
- At least 2 years of on-site monitoring experience.
- Good knowledge of and skill in applying applicable clinical research regulatory requirements.
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint.
- Written and verbal communication skills including good command of the English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
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