Clinical Data Associate II

Job Description: As a Clinical Data Associate II, you will provide data management support and assistance throughout the clinical trial data management process for assigned projects under direct supervision. You will be responsible for following Standard Operating Procedures (SOPs), regulatory directives, study specific plans, and guidelines. Your duties will include supporting the Lead DM, performing data entry for paper-CRF studies, conducting quality control of data entry, developing CRF specifications, assisting in building clinical databases, maintaining quality controlled database build documentation, specifying requirements for edit check types, creating and revising data management documentation, training clinical research personnel, reviewing and querying clinical trial data, running status and metric reporting, performing medical coding, assisting in SAE/AE reconciliation, liaising with third-party vendors, and potentially assisting with SAS programming. Key Responsibilities: - Support the Lead DM and perform data entry for paper-CRF studies - Conduct quality control of data entry and develop CRF specifications - Assist in building clinical databases and maintain quality controlled database build documentation - Specify requirements for edit check types and create/revise data management documentation - Train clinical research personnel and review/query clinical trial data - Run status and metric reporting, perform medical coding, and assist in SAE/AE reconciliation - Liaise with third-party vendors and may assist with SAS programming Qualifications Required: - Bachelor's degree or a combination of related experience - Minimum of 2 years of experience in data management - Proficiency in Microsoft Office - Excellent organizational and communication skills - Professional use of the English language - Experience in a clinical, scientific, or healthcare discipline is preferred,