Title: Global Study Specialist

Duration: 12-month contract with extensions (Multi-year engagement)

Location: Remote (must sit in Canada – EST)

Must-Haves:

• 1+ year of clinical trial experience (pharma/life sciences)
• Oncology clinical trial experience
• Experience supporting clinical trials from start-up through closeout
• Strong documentation experience (eTMF / CTMS)
• Experience working with CROs
• Experience adhering to ICH-GCP guidelines
• Ability to manage multiple studies at different phases simultaneously
• Experience meeting tight deadlines in a fast-paced environment
• Submissions experience (regulatory / ethics committees)
• Bachelor’s degree (life sciences or related)

Day-to-Day:

• Support clinical trials from start-up through closeout
• Manage and maintain study d...