Clinical data management

As a Data Entry Assistant in this role, you will be responsible for supporting the data management processes of clinical trial data in accordance with Good Clinical Data Management Practices (GCDMP). Your key tasks will include assisting in data entry, validation, and cleaning procedures to ensure accuracy and compliance. You will also play a crucial role in aiding the development and testing of Case Report Forms (CRFs) and electronic data capture (EDC) systems. Additionally, you will be tasked with managing discrepancies and data queries efficiently to address any data issues that may arise during the process. Maintaining detailed study-specific documentation, such as data management plans and data validation guidelines, will be part of your responsibilities. Collaboration with diverse teams including clinical research associates, biostatisticians, and programmers will be essential to ensure seamless data management operations. Furthermore, you will be involved in activities related to database lock and archiving, as well as participating in quality control procedures and audits to uphold data integrity standards. It will be imperative for you to familiarize yourself with and adhere to standard operating procedures (SOPs), ICH-GCP guidelines, and regulatory principles pertinent to clinical data management. This position offers full-time, permanent employment opportunities, making it an ideal fit for individuals looking to establish a career in data management within the clinical research domain. In addition to a dynamic work environment, the role comes with benefits such as health insurance and paid sick time. Please note that the work location for this position is on-site, requiring your presence in person to fulfill the responsibilities effectively.,