IQVIA is seeking a Clinical Research Associate to conduct site monitoring visits and ensure protocol adherence across sites. You will drive recruitment plans, train site staff, and maintain regular communication to manage expectations and resolve issues.
The role requires GCP/ICH knowledge, strong organizational skills, and proficiency in Word, Excel and PowerPoint. On-site collaboration with teams ensures quality data and regulatory compliance.
#J-18808-Ljbffr
Senior CRA: Single-Sponsor Clinical Monitoring employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.
