Data Management Associate

You will be responsible for collecting and entering clinical trial data from various sources, ensuring that it complies with study protocols and regulatory standards. Additionally, you will review the data for discrepancies, missing values, and inconsistencies, perform data cleaning, and uphold data quality standards. You will also be tasked with identifying, escalating, and resolving data queries in collaboration with clinical teams and study sites. In this role, you will maintain and manage essential study documents such as case report forms (CRFs), data management plans, and databases. Effective collaboration with Clinical Research Associates (CRAs), Clinical Data Managers, and other stakeholders is essential to ensure the timely and accurate collection of data. Furthermore, you will provide support for the maintenance and configuration of data management systems and software to guarantee the smooth flow of data. This position is full-time and requires work to be conducted in person. The benefits offered for this position include health insurance.,