• Performing all data management deliverables for assigned studies • Attending and participating in client meetings as requested • Understanding study requirements for implementation and data collection • Collaborating with project teams to develop study-specific edit check criteria • Defining, running, and reviewing edit checks and resolving discrepant data • Maintaining organized, complete, and up-to-date study documentation • Performing study setup activities, including database structure, specifications, and approvals • Coordinating and documenting the receipt and processing of electronic or ancillary data received from external sources such as central laboratories, CROs, or sponsors • Keeping supervisors informed of project status and potential issues • Ensure the accuracy and consistency of clinical databases by: • Reviewing clinical data and identifying errors or inconsistencies • Collaborating with project teams to resolve data issues • Tracking outstanding issues and following up until resolution • Ensuring that clinical data management activities comply with regulatory guidelines and study protocols • Additional responsibilities: • Adhere to Clinical Data Management procedures, policies, and work instructions • Read, understand, and follow applicable Standard Operating Procedures (SOPs) • Assist in establishing and maintaining departmental standards • Participate in the review and update of company SOPs related to Data Management services • Work with internal teams to resolve issues and support operational goals • Contribute to team success by supporting colleagues and sharing knowledge • Participate in company-sponsored training and maintain awareness of industry best practices • Perform additional tasks and responsibilities as assigned