Description
The Senior Clinical Data Associate provides data management support for assigned clinical trial projects from study start-up through post-database lock, working under direct supervision. The role supports the Lead Data Manager, performs data entry and quality control, develops and tests clinical databases, creates and maintains data management documentation, reviews and queries clinical data, supports SAE/AE reconciliation, coordinates with vendors, and may assist with SAS programming and protocol or study report review. The position requires at least five years of experience, a bachelor's degree or related experience, Microsoft Office proficiency, and knowledge of ICH-GCP, precision oncology SOPs, and regulatory guidance; travel may be required.
