Clinical Research Associate

Responsibilities: Ensure study activities reflect Johnson & Johnson Credo Values and protect subject safety at assigned sites Support operational execution of clinical trials and high-quality data collection Follow SOPs, GCP, and regulatory requirements in trial activities Be accountable for site performance and data quality within project timelines Assist operations staff and site staff in resolving issues and implementing corrective actions Verify Investigator Site Files comply with regulations and company procedures Support patient recruitment and retention efforts Conduct site visits to ensure protocol and regulatory compliance Facilitate internal communication of critical clinical data and events Assist with Investigator and site training logistics if needed Maintain up-to-date knowledge of site status for stakeholders Understand and balance business objectives with functional needs in clinical projects May participate in additional Clinical Operations tasks and new system/process implementations Collaborate with Investigators, IRBs/ECs, vendors, and company personnel as required Comply with Health Care Compliance Program and Code of Conduct in all activities Provide additional support to Clinical Operations staff as needed Key requirements communication problem solving cross-functional collaboration compliance with SOPs and GCP regulatory knowledge (federal, state, local) clinical site monitoring and data quality