Clinical Data Associate

I'm partnering with an innovative biotechnology company seeking a Clinical Data Associate (CDA) to support clinical studies through data management activities, data review, discrepancy management, database quality control, and vendor data reconciliation. This is an excellent opportunity for someone with clinical data management experience who enjoys working in a collaborative, fast-paced clinical development environment. Requirements Associate's degree or higher 2+ years of clinical data management experience within a biotech, pharmaceutical, or CRO environment Hands-on experience with Electronic Data Capture (EDC) systems Experience with Medidata Rave preferred Strong organizational, communication, and problem-solving skills Experience working in cross-functional clinical study teams Responsibilities Support maintenance and updates of Data Management Plans, Data Validation Plans, Data Review Plans, and CRF Completion Guidelines Review and verify external vendor data according to study specifications Generate, review, and track study data metrics and reports Participate in ongoing data review activities Review, manage, and resolve data discrepancies within EDC systems Perform external data reconciliations, including Serious Adverse Event (SAE) reconciliation Conduct database quality control activities and support database review processes Track data issues and communicate trends to study teams for follow-up Ensure compliance with company procedures, GCP guidelines, and regulatory requirements Maintain study documentation and support Trial Master File (TMF) activities Preferred Experience with Medidata Rave Experience supporting multiple clinical studies simultaneously Strong understanding of GCP and clinical data management best practices #J-18808-Ljbffr