Clinical Researcher Coordinator

Summary

Join BizForce as a Clinical Research Coordinator and play a key role in supporting our research team by handling data entry, documentation, and coordination tasks crucial to the success of ongoing and future Hepatology studies. Manage and coordinate clinical trial activities, perform accurate data entry, maintain compliant study documentation, collaborate with research teams, monitor data quality, assist with patient recruitment, prepare reports, and ensure protocol adherence. This remote position requires a minimum of 3 years of clinical trial experience (Hepatology preferred), strong understanding of ICH-GCP guidelines, excellent attention to detail, proficiency in clinical trial software, and strong communication skills. BizForce offers a permanent work-from-home arrangement, leave credits, monetary allowance, annual bonus, weekly paychecks, fixed weekends off, a thriving company culture, specialized training programs, and a highly competitive salary.

Requirements

• Minimum 3 years’ experience in a clinical trial setting (Hepatology experience strongly preferred)
• Strong understanding of ICH-GCP guidelines and regulatory requirements
• Excellent attention to detail, organizational, and problem-solving skills
• Proficient in clinical trial software, ECW system, and Microsoft Office tools
• Ability to work independently and manage multiple priorities in a remote environment
• Strong communication skills for cross-functional collaboration
• Amenable to work during U.S. business working hours

Responsibilities

• Manage and coordinate clinical trial activities specific to Hepatology research projects
• Perform accurate and timely data entry into clinical trial databases and electronic data capture systems
• Maintain detailed and compliant study documentation, including regulatory forms, trial master files, and patient records
• Collaborate with principal investigators, research nurses, and data management teams to ensure protocol adherence
• Monitor data quality and resolve discrepancies in accordance with Good Clinical Practice (GCP) and study requirements
• Assist with patient recruitment, informed consent processes, and follow-up communications (as required)
• Prepare and submit reports for study progress and regulatory compliance

Benefits

• Permanent Work From Home
• Leave Credits
• Monetary Allowance
• Annual Bonus
• Weekly Paychecks
• Fixed Weekends Off
• Thriving Company Culture with Complete Autonomy
• Exclusive Specialized Training Programs