Temporary Research Coordinator - Clinical Trials

Become a Temporary Research Coordinator with expertise in clinical trials, focusing on APOL1 Mediated Kidney Disease research. Utilize your skills in data management, ethics compliance, and patient interaction. In this role, you'll play a vital part in facilitating a clinical trial at an ambulatory care hospital.

Responsibilities include managing the application processes with the Research Ethics Board, developing study-related documentation, and ensuring timely communication within the research team. Your proactive nature and attention to detail will help maintain smooth lab operations and study protocols. Key Responsibilities:

• Coordinate recruitment and assessment for study participants
• Manage and submit ethics applications and track approvals
• Create informed consent forms and study questionnaires
• Organize procurement and follow-up of biological specimens
• Generate and submit research progress reports Requirements:
• Bachelor's degree in Public Health or related discipline
• Minimum 3 years’ experience in clinical trials
• Familiarity with research planning and management processes
• Proficient in data management tools and MS Office
• Strong communication and analytical skills Support vital clinical research efforts focused on kidney health while ensuring adherence to safety standards and best practices.