Regulatory Associate (Pharmaceutical submissions)
ClinChoice(13 days ago)
About this role
Regulatory Associate Consultant focused on pharmaceutical submissions supporting a major pharmaceutical client through ClinChoice. Hybrid position based in Toronto, Ontario for a 12-month contract within a global CRO environment.
Required Skills
- Regulatory Submissions
- eCTD
- Labeling
- Submission Management
- Project Management
- Regulatory Knowledge
- Lifecycle Management
- Regulatory Systems
- Communication
- Problem Solving
Qualifications
- B.Sc. in Biological Sciences
About ClinChoice
clinchoice.comClinChoice is a full‑service global contract research organization (CRO) that helps accelerate drug and medical device approvals to market. They offer end‑to‑end clinical development, regulatory strategy, and operational support across study design, execution, data management and safety to guide sponsors through all phases of development. With global site networks, therapeutic expertise and data‑driven processes, ClinChoice aims to shorten timelines and reduce risk for development programs. They partner with biotech, pharma and device companies to navigate complex regulatory pathways and bring safer products to patients.
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