About the Role
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...
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