ICON Strategic Solutions seeks a Clinical Trial Associate focused on oncology in a hybrid role in Mississauga. Leverage your clinical research skills in a supportive workplace dedicated to patient outcomes. As a Clinical Trial Associate, you will play a crucial role in coordinating clinical trials, ensuring compliance with all regulations, and maintaining trial documentation.
Your efforts will directly support the execution of groundbreaking oncology studies that improve patient lives. Collaborate with interdisciplinary teams to facilitate effective communication and analyze trial metrics. Key Responsibilities:
Coordinate and administer clinical trials effectively
Organize and oversee all trial documentation
Prepare informed consent forms and maintain study materials
Collaborate with teams to ensure smooth trial processes
Report metrics and milestones regarding the clinical trials Requirements:
Bachelor's degree in a scientific or healthcare discipline
Relevant experience in clinical research preferred
Familiarity with clinical trial processes and regulations
Solid organizational and communication abilities
Experience in oncology studies necessary Utilize your skills in clinical trial management to contribute to cutting-edge research at ICON in Mississauga.