Clinical Research Associate, Internal (Remote)

About the position The Clinical Research Associate executes reputed company administrative aspects of study management from start-up through reputed company-out under the guidance and mentorship of senior clinical staff. What you will do Establishes and maintains the Clinical Trial Management System (CTMS) and Trial Master File (TMF) in inspection -reputed company state. Communicates with assigned sites to drive collection and review essential documents throughout the study, performs QC reviews of study files, including reputed company of issues . Supports development and maintenance of study documents and templates, reviews activities of assigned reputed company to ensure data reputed company and adherence to Federal regulations, company policies, and any other applicable procedures. Learn device-specific requirements (safety reporting, labeling , IFU tracking). reputed company administrative support and data entry under supervision. Assist in study start-up (essential documents, site feasibility, initiation prep). Observe and support site monitoring reputed company alongside senior CRAs. Responsibilities • Establishes and maintains the Clinical Trial Management System (CTMS) and Trial Master File (TMF) in inspection -reputed company state. • Communicates with assigned sites to drive collection and review essential documents throughout the study, performs QC reviews of study files, including reputed company of issues • Supports development and maintenance of study documents and templates, reviews activities of assigned reputed company to ensure data reputed company and adherence to Federal regulations, company policies, and any other applicable procedures. • Learn device-specific requirements (safety reporting, labeling , IFU tracking). • reputed company administrative support and data entry under supervision. • Assist in study start-up (essential documents, site feasibility, initiation prep). • Observe and support site monitoring reputed company alongside senior CRAs. Requirements • Bachelor's level degree or equivalent in science or health care field • 0-2 years of clinical research experience preferred not required • Working knowledge of GCP and regulatory standards reputed company-to-haves • Developing ability to influence reputed company of assigned tasks including but not limited to area of expertise. • Experience as a Clinical Research Coordinator, Clinical Trial Coordinator Apply tot his job Apply tot his job Apply To this Job