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Clinical Trials Specialist
2 months ago
Job Summary
The Clinical Trials Specialist will play a key role in the development, coordination, and management of clinical trials at the Canadian Myeloma Research Group. This position will be responsible for a wide range of projects, including protocol development, clinical trial monitoring, and data management.
Key Responsibilities
- Study management and coordination
- Clinical trial monitoring and data management
- Protocol development and writing
- Regulatory compliance and communication with sponsors and sites
- Quality assurance and data integrity
Requirements
- Experience in clinical trials management and monitoring
- Proficiency in English and French, with excellent communication skills
- Strong organizational and prioritization skills
- Ability to work under pressure and meet deadlines
- Knowledge of applicable legislative and regulatory policies
Preferred Qualifications
- SoCRA or ACRP designation
- Experience with Medidata Rave and MS Office Suite
Working Conditions
This is a full-time position that requires up to 70% travel.