Steer clinical research projects focused on kidney health as a Clinical Research Coordinator. Manage participant engagement, regulatory submissions, and ensure compliance with research protocols.
As a vital member of the research team, you will coordinate both industry and grant-funded trials. Your responsibilities will span from drafting ethics applications to data oversight and participant monitoring. Strong organizational skills and attention to detail are essential for managing the comprehensive documentation involved in clinical trials.
Key Responsibilities:
• Conduct and manage the full cycle of clinical trials
• Develop ethics applications and manage consent processes
• Identify and recruit potential study participants
• Maintain thorough study files and documentation
• Communicate regularly with principal investigators
Requirements:
• Relevant clinical research experience or education
• Proficient in Microsoft Office applications
• Ability to pr...