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 environment 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
- Strong 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.