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Clinical Trials Specialist

2 months ago


Vaughan, Ontario, Canada Canadian Myeloma Research Group Full time

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.