Base: $50,648 – $63,310 cad; bonus/equity: not spe...
Hybrid
Oncology clinical research experience required
Strong understanding of regulatory documentation
Knowledge of clinical trial processes and regulations
The role involves assisting in the coordination and administration of clinical trials while ensuring compliance with protocols and regulatory requirements
Job Summary
The role involves assisting in the coordination and administration of clinical trials while ensuring compliance with protocols and regulatory requirements.
ICON plc fosters an inclusive environment driving innovation and excellence in shaping the future of clinical development.
The position offers competitive benefits including health insurance, retirement planning, and global employee assistance programs.
Matching Summary
The role involves assisting in the coordination and administration of clinical trials while ensuring compliance with protocols and regulatory requirements.
Salary
Base: $50,648 – $63,310 CAD; Bonus/Equity: Not specified; Benefits: Health insurance, retirement planning, annual leave
Skills & Requirements
Must-have
Oncology clinical research experience required
Strong understanding of regulatory documentation
Knowledge of clinical trial processes and regulations
Nice-to-have
Excellent organizational and communication skills
Ability to work in a fast-paced environment
Interest in clinical development innovation
Key Requirements
Bachelor's degree in scientific or healthcare-related field
Two years experience in Clinical Research
Must be comfortable with hybrid role in Mississauga Canada