Clinical Trials Coordinator

Benefits

Qualifications

• •We are seeking a dedicated and experienced Clinical Trial Coordinators with phlebotomy certificate and has experience in Phase 1, 2 and 3 clinical trials.
• •The ideal candidate will possess a strong background in clinical research, ensuring compliance with FDA regulations and maintaining high standards throughout the trial process
• •Proven experience in clinical research management with a strong understanding of clinical trials management processes
• •Knowledge of FDA regulations and GCP guidelines is essential
• •Familiarity with data management practices in a clinical setting
• •Experience in patient monitoring techniques within clinical trials
• •Strong organizational skills with the ability to manage multiple projects simultaneously
• •Excellent communication skills for effective collaboration with diverse teams
• •Gastroenterology
• •Rialto, CA 92377 (Required)
• •7 more items(s)

Responsibilities

• •This role is crucial for the successful execution of clinical studies, focusing on patient monitoring, data management, and collaboration with cross-functional teams
• •Plan, initiate, and manage clinical trials in accordance with regulatory requirements and company policies
• •Develop study protocols, informed consent forms, and case report forms
• •Ensure adherence to Good Clinical Practice (GCP) and FDA regulations throughout the trial lifecycle
• •Oversee patient recruitment, monitoring, and retention strategies to ensure optimal participant engagement
• •Collaborate with clinical laboratories to ensure accurate data collection and analysis
• •Manage study budgets, timelines, and resources effectively to meet project milestones
• •Conduct regular site visits to monitor trial progress and address any issues that arise
• •Facilitate communication between stakeholders including sponsors, investigators, and regulatory authorities
• •Prepare reports on trial progress for internal teams and external stakeholders
• •7 more items(s)