Become a Study Start-Up Specialist and lead site activation from initial phases to completion.

Your role is critical in managing compliance and facilitating smooth study operations. You will be responsible for supporting operational activities across various investigator sites, ensuring compliance with clinical trial timelines and applicable regulations. Your expertise in preparing Investigator Initiation Packages and resolving issues will enhance the site activation process. Collaboration with regulatory teams will also be vital for meeting submission requirements. Key Responsibilities:

- Initiate management of Investigator Initiation Package documentation
- Address and escalate any site-related issues promptly




- Coordinate with other teams to ensure site activation
- Engage with regulatory groups for necessary documentation
- Keep clinical trial systems updated with compliance data Requirements:
- Diploma or bachelor’s in life sciences preferred
- At least 2 years of experience in clinical trials
- Knowledge in pharmaceutical or CRO setting is beneficial
- Understanding of ICH/GCP and FDA regulations
- Fluent in English and local language Apply your clinical trial expertise in this vital role to ensure successful study activation and compliance.

📌 Study Start-Up Specialist Opportunity (Canada)
🏢 Parexel International
📍 Canada