Clinical Research Manager

Protocol Design: Collaborates with researchers to develop clear study rules and testing plans. Site Management: Selects and evaluates clinical trial locations and coordinates vendor contracts. Budgeting: Allocates and manages trial funds, ensuring cost-effective operations. Equipment & Supplies: Ensures testing facilities are properly equipped and supplied for participant visits. Compliance & Ethics Regulatory Oversight: Prepares and submits documents to the Institutional Review Board and regulatory agencies. Protocol Adherence: Enforces strict adherence to Good Clinical Practice guidelines set by the FDA. Patient Safety: Implements safety measures and risk assessments to protect patient rights and well-being. Staff Supervision: Manages Clinical Research professionals Performance Evaluation: Trains team members, evaluates their work, and conducts coaching sessions. Meeting Facilitation: Organizes regular meetings with doctors, nurses, and sponsors to review progress. Data & Trial Monitoring Participant Enrollment: Oversees the recruitment and screening of study subjects. Data Quality: Conducts routine audits of trial data to ensure accuracy and resolve discrepancies. Record Keeping: Maintains organized and audit-ready electronic files. Adverse Event Reporting: Monitors patients for side effects and documents all negative medical reactions. #J-18808-Ljbffr