Centralized Monitor Professional

Essential Functions:

• Independently manage assigned sites and perform Subject Level Data Review; perform dual roles if required.
• Conduct remote monitoring visits as assigned.
• Investigate clinical data at the site level to ensure accuracy and completeness of patient information for reviews.
• Engage in study-specific analytics and contribute to developing new analytics proposals as per customer demand.
• Provide operational insights on assigned sites/studies, manage study/site metrics, and ensure compliance with clinical operation plans.
• Offer guidance and input to clinical study teams and stakeholders to facilitate continuous process improvements and issue resolution.

Qualifications:

• Bachelors degree in clinical, life sciences, mathematical sciences, related field, or nursing.
• At least 2 years of relevant experience or an equivalent combination of education, training, and experience.

This role ensures the smooth execution of clinical trials with a focus on quality and efficacy, supporting IQVIAs commitment to enhancing healthcare outcomes.